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510(k) K014121

WARMTOUCH CARDIAC BLANKET,CATALOG # 503-0860 by Nellcor Puritan Bennett, Inc. — Product Code DWJ

K014121 is an FDA 510(k) premarket notification submitted by Nellcor Puritan Bennett, Inc. for the device "WARMTOUCH CARDIAC BLANKET,CATALOG # 503-0860". The FDA issued a decision of Substantially Equivalent on January 11, 2002. The device falls under product code DWJ (System, Thermal Regulating), a Class II device regulated under 21 CFR 870.5900. Nellcor Puritan Bennett, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 11, 2002
Date Received
December 17, 2001
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Thermal Regulating
Device Class
Class II
Regulation Number
870.5900
Review Panel
CV
Submission Type

If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

Other clearances by Nellcor Puritan Bennett, Inc.

  • K070899 — PURITAN BENNETT LEGENDAIR XL2 (December 13, 2007)
  • K070408 — DURAMAX REUSABLE OXIMETRY SENSOR (May 25, 2007)
  • K060576 — NELLCOR OXIMAX N-600X PULSE OXIMETER (August 14, 2006)
  • K051271 — OXIMAX NEOMAX ADHESIVE FOREHEAD REFLECTANCE OXIMETRY SENSOR (January 10, 2006)
  • K052186 — NELLCOR OXIMAX PULSE OXIMETRY SENSONS (MAX-A, MAX-AL, MAX-N, MAX-I, MAX-P (November 10, 2005)
  • K051352 — OXIMAX NPB-40 HANDHELD PULSE OXIMETER (August 11, 2005)
  • K050072 — GOODKNIGHT 425ST (June 13, 2005)
  • K033973 — OXISENSOR II RECYCLED SENSOR AND OXIMAX RECYCLED SENSOR (December 13, 2004)
  • K030787 — SHILEY FLEXTRA TRACHEOSTOMY TUBE (November 14, 2003)
  • K030930 — OXIMAX SOFTCARE SENSORS, MODELS SC-A, SC-PR, SC-NEO, SC-N (May 23, 2003)

Other clearances for product code DWJ

  • K262089 — Disposable Warming Blanket (August 21, 2026)
  • K261437 — Mistral-Air® Warming System (August 7, 2026)
  • K260278 — ThermAffyx(TM) Patient Safety System (July 8, 2026)
  • K260903 — Hot Pink Pad Warming System (April 16, 2026)
  • K252861 — Warming System (April 7, 2026)
  • K251974 — Arctic Sun Temperature Management System (Model 5000) (October 24, 2025)
  • K242964 — Celsi Warmer (June 20, 2025)
  • K243942 — Arctic Sun Stat Temperature Management System (April 30, 2025)
  • K232627 — HotDog Warming Mattress + Return Electrode (April 18, 2024)
  • K232502 — Cocoon Convective Warming System, Model CWS7000 (February 21, 2024)

FDA data resources