Cleared Traditional

K902749 - OLYMPIC MINI BILI-LITE, MODEL 77

K902749 is an FDA 510(k) clearance for OLYMPIC MINI BILI-LITE, manufactured by Olympic Medical Corp.. The device is a Class 2 General Hospital device with product code LBI cleared through the Traditional 510(k) pathway after a 41-day FDA review.

K902749 · Olympic Medical Corp. · General Hospital
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Aug 1990
Decision
41d
Days
Class 2
Risk

K902749 is an FDA 510(k) clearance for the OLYMPIC MINI BILI-LITE, MODEL 77. Classified as Unit, Neonatal Phototherapy (product code LBI), Class II - Special Controls.

Submitted by Olympic Medical Corp. (Seattle, US). The FDA issued a Cleared decision on August 2, 1990 after a review of 41 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5700 - the FDA general hospital device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Olympic Medical Corp. devices

FDA 510(k) Submission Details - K902749

510(k) Number K902749 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 22, 1990
Decision Date August 02, 1990
Days to Decision 41 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
88d faster than avg
Panel avg: 129d · This submission: 41d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LBI Device Classification - Class 2, Special Controls

Product Code LBI Unit, Neonatal Phototherapy
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5700
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General Hospital devices follow this clearance model.

Regulatory Peers - LBI Unit, Neonatal Phototherapy

All 30
Devices cleared under the same product code (LBI) and FDA review panel - the closest regulatory comparables to K902749.
OLYMPIC BILI-LITE
K940996 · Olympic Medical Corp. · Sep 1994
BILIBLANKET LIGHT METER
K910571 · Ohmeda Medical · Jul 1992
OLYMPIC BILI-METER(TM) WITH TYPE-F SENSOR
K903445 · Olympic Medical Corp. · Oct 1990
OLYMPIC BILI-LITE-PAD(TM)
K901987 · Olympic Medical Corp. · Jul 1990
BILIBLANKET PHOTOTHERAPY DEVICE
K894129 · Ohmeda Medical · Sep 1989
AEQUITRON MED-7100 PHOTOTHERAPY LIGHT
K850181 · Aequitron Medical, Inc. · Apr 1985