Olympic Warm-Bassinet

No FDA recalls found in the data synced 9 Oct 2026.

510(k) Number

K954216 ↗

FDA Product Code

FOH

Device Class

Class I

Regulation

21 CFR Part 880.5560

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Olympic Smart Scale Care Center

  Class II

  FDA 510(k) K920423 Active Cleared 11 Jun 1992

• Olympic Medical Lectromed Cerebral Function Monitor System, Model 5330

  Class II

  FDA 510(k) K020335 Active Cleared 18 Jun 2002

• Lube-Lok

  Class I

  FDA 510(k) K781695 Active Cleared 1 Nov 1978

• Olympic Bili-Lite-Pad(Tm)

  Class II

  FDA 510(k) K901987 Active Cleared 16 Jul 1990

• Olympix Mini-Pasteurmatic (58210)

  Class II

  FDA 510(k) K972193 Active Cleared 5 Sep 1997

• Warm-Scale

  Class I

  FDA 510(k) K952649 Active Cleared 15 Aug 1995

See all devices from Olympic Medical Corp. →