Cleared Traditional

K901522 - OLYMPIC SMART SCALE PEDIATRICS MODEL 50

K901522 is an FDA 510(k) clearance for OLYMPIC SMART SCALE PEDIATRICS MODEL 50, manufactured by Olympic Medical Corp.. The device is a Class 1 General Hospital device with product code FRW cleared through the Traditional 510(k) pathway after a 81-day FDA review.

K901522 · Olympic Medical Corp. · General Hospital
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Jun 1990
Decision
81d
Days
Class 1
Risk

K901522 is an FDA 510(k) clearance for the OLYMPIC SMART SCALE PEDIATRICS MODEL 50. Classified as Scale, Patient (product code FRW), Class I - General Controls.

Submitted by Olympic Medical Corp. (Seattle, US). The FDA issued a Cleared decision on June 22, 1990 after a review of 81 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.2720 - 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 - K901522

510(k) Number K901522 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 02, 1990
Decision Date June 22, 1990
Days to Decision 81 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
48d faster than avg
Panel avg: 129d · This submission: 81d
Pathway characteristics
Predicate-based equivalence.

FRW Device Classification - Class 1, General Controls

Product Code FRW Scale, Patient
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.2720
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - FRW Scale, Patient

All 13
Devices cleared under the same product code (FRW) and FDA review panel - the closest regulatory comparables to K901522.
3M MODEL 200RT RATE TAPER INFUSION PUMP
K926059 · 3M Health Care, Ltd. · Aug 1993
SMART SCALE X-RAY PLATFORM
K904138 · Olympic Medical Corp. · Nov 1990
VAAKA BABY SCALE
K902545 · Ferguson Medical · Jul 1990
OLYMPIC SMART SCALE
K871104 · Olympic Medical Corp. · May 1987
WARM WEIGH MODEL N-10 INFANT SCALE
K870888 · Air-Shields, Inc. · Mar 1987
MODEL 304-S EXTERNAL MICRO-VOLUME INFUSION PUMP
K864327 · Medtronic Minimed · Feb 1987