Cleared Traditional

K813408 - SAGE 2200 STERILE SPECIMEN CONTAINER

K813408 is an FDA 510(k) clearance for SAGE 2200 STERILE SPECIMEN CONTAINER, manufactured by Sage Products, Inc.. The device is a Class 2 Radiology device with product code FMT cleared through the Traditional 510(k) pathway after a 49-day FDA review.

K813408 · Sage Products, Inc. · Radiology device
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Jan 1982
Decision
49d
Days
Class 2
Risk

K813408 is an FDA 510(k) clearance for the SAGE 2200 STERILE SPECIMEN CONTAINER. Classified as Warmer, Infant Radiant (product code FMT), Class II - Special Controls.

Submitted by Sage Products, Inc. (Mchenry, US). The FDA issued a Cleared decision on January 25, 1982 after a review of 49 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 880.5130 - the FDA radiology and imaging software oversight 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 Sage Products, Inc. devices

FDA 510(k) Submission Details - K813408

510(k) Number K813408 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 07, 1981
Decision Date January 25, 1982
Days to Decision 49 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
58d faster than avg
Panel avg: 107d · This submission: 49d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FMT Device Classification - Class 2, Special Controls

Product Code FMT Warmer, Infant Radiant
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5130
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 Radiology devices follow this clearance model.

Regulatory Peers - FMT Warmer, Infant Radiant

All 60
Devices cleared under the same product code (FMT) and FDA review panel - the closest regulatory comparables to K813408.
OHIO 3000 INFANT WARMER SYSTEM
K840857 · Ohio Medical Products · Mar 1984
OHIO 3300 INFANT WARMER SYSTEM
K840858 · Ohio Medical Products · Mar 1984
RESUSCITAIRE
K830748 · Vickers America Medical Corp. · Jun 1983
WARMING LISTHTS #96H & 96HT
K812745 · J. H. Emerson Co. · Nov 1981
OHIO RADIANT WARMER
K802365 · Ohio Medical Products · Oct 1980
INFANT CARE SYSTEM
K790137 · Narco Air-Shields · Mar 1979