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510(k) K870382

DRV DISP RESUSCIT 3000/BAG ADAPT 3010 & 3011 by Nova-Ventrx — Product Code CBP

K870382 is an FDA 510(k) premarket notification submitted by Nova-Ventrx for the device "DRV DISP RESUSCIT 3000/BAG ADAPT 3010 & 3011". The FDA issued a decision of Substantially Equivalent on March 6, 1987. The device falls under product code CBP (Valve, Non-Rebreathing), a Class II device regulated under 21 CFR 868.5870. Nova-Ventrx has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 6, 1987
Date Received
January 29, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Valve, Non-Rebreathing
Device Class
Class II
Regulation Number
868.5870
Review Panel
AN
Submission Type

Other clearances by Nova-Ventrx

  • K952267 — CRITERION, CRITERION I.V., MODIFIED (December 2, 1997)
  • K954480 — CONDENSATE COLLECTION KIT (December 29, 1995)
  • K893760 — CRITERION I.V. VENTILATOR BREATHING CIRCUIT #1004 (August 10, 1989)
  • K881207 — RES-Q 1, 2, 3, 4 AND 5 (August 15, 1988)
  • K863756 — MODIFIED CRITERION VENTILATOR BREATHING CIRCUIT (November 13, 1986)
  • K850600 — CO-AX VENTILATOR CIRCUIT (May 2, 1985)
  • K842794 — MAXI-MISER HUMIDIFIER INSERT 1020 & 1021 (October 4, 1984)
  • K842795 — MAXI-MISER HUMIDIFIER INSERT 1030 (October 4, 1984)
  • K841569 — MAXI-MISER HUMIDIFIER INSERT 1020 (May 30, 1984)
  • K841571 — MAXI-MISER WATER TRANSFER SET 1021/1022 (May 30, 1984)

Other clearances for product code CBP

  • K241366 — QualityFlow O2 Series (QualityFLOW O2); QualityFlow O2 Series (QualityFLOW O2 MT (October 29, 2024)
  • K234053 — F&P Optiflow Flow Diverter (August 9, 2024)
  • K210992 — Altech® Exhalation Valve (Single Limb and Dual Limb) (December 23, 2021)
  • K192285 — CPR Face Shield (November 25, 2020)
  • K173770 — OJR215 Pressure Relief Manifold (April 5, 2019)
  • K171961 — Compower CPR Mask With Oxygen Port, Compower CPR Mask Without Oxygen Port, Compo (November 17, 2017)
  • K152521 — Seal Rite Non-Rebreathing Valve (June 3, 2016)
  • K142764 — KYOLING CPR Mask with Oxygen Port and Without Oxygen Port (July 9, 2015)
  • K142402 — BigEasy Non-Rebreathing Valve (March 23, 2015)
  • K132143 — EXHALATION VALVE (June 4, 2014)

FDA data resources