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510(k) K935098

BABY BOARD by Sentry Medical Products, Inc. — Product Code BTX

K935098 is an FDA 510(k) premarket notification submitted by Sentry Medical Products, Inc. for the device "BABY BOARD". The FDA issued a decision of Substantially Equivalent on February 15, 1994. The device falls under product code BTX (Board, Arm (With Cover), Sterile), a Class I device regulated under 21 CFR 878.3910. Sentry Medical Products, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 15, 1994
Date Received
October 25, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Board, Arm (With Cover), Sterile
Device Class
Class I
Regulation Number
878.3910
Review Panel
SU
Submission Type

Other clearances by Sentry Medical Products, Inc.

  • K962122 — SENTRY RADIOTRANSLUCENT ECG ELECTRODES (July 24, 1996)
  • K955636 — SENTRY DISPOSABLE DISPERSIVE ELECTRODE (March 27, 1996)
  • K942827 — SENTRY INSERTION TRAY (November 2, 1994)
  • K934000 — SENTRY AQUEOUS GEL ECG ELECTRODES (August 30, 1994)
  • K933603 — LEADWIRE (January 18, 1994)
  • K932704 — PATIENT CABLE (December 27, 1993)
  • K881670 — ACCUTEMP PLUS (November 22, 1988)
  • K881343 — DURADERM BUTTERFLY (May 4, 1988)
  • K851522 — DIAGNOSTIC ECG DISPOSABLE ELECTRODE (October 24, 1985)
  • K853552 — SENTRY FLEXIBLE TENS (September 26, 1985)

Other clearances for product code BTX

  • K900175 — 4/1 ARMBOARD (January 24, 1990)
  • K884838 — ALLEN PRONE ARMBOARD (December 15, 1988)
  • K882524 — UNIVERSALLY ADJUSTABLE ARMBOARD (July 8, 1988)
  • K881292 — ALLEN LATERAL ARMBOARD (April 7, 1988)
  • K864670 — BOARD, ARM (WITH COVER) (January 12, 1987)
  • K833664 — ARMBOARD AND THE BOARD (December 27, 1983)
  • K830018 — SAFE-T ARM BOARD (January 26, 1983)
  • K823412 — ARM BOARD W/I.V COVERING (December 15, 1982)
  • K811419 — SPRIO-LOOP (June 12, 1981)
  • K792147 — ARM SHIELD FOR ANESTHESIA (December 6, 1979)

FDA data resources