Cleared Traditional

K801333 - AMPCO DRESSING CHANGE TRAYS

K801333 is an FDA 510(k) clearance for AMPCO DRESSING CHANGE TRAYS, manufactured by Associated Medical Products Co.. The device is a Class 2 General Hospital device with product code FRG cleared through the Traditional 510(k) pathway after a 80-day FDA review.

K801333 · Associated Medical Products Co. · General Hospital
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Aug 1980
Decision
80d
Days
Class 2
Risk

K801333 is an FDA 510(k) clearance for the AMPCO DRESSING CHANGE TRAYS. Classified as Wrap, Sterilization (product code FRG), Class II - Special Controls.

Submitted by Associated Medical Products Co. (Walker, US). The FDA issued a Cleared decision on August 22, 1980 after a review of 80 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6850 - 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 Associated Medical Products Co. devices

FDA 510(k) Submission Details - K801333

510(k) Number K801333 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 03, 1980
Decision Date August 22, 1980
Days to Decision 80 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
49d faster than avg
Panel avg: 129d · This submission: 80d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FRG Device Classification - Class 2, Special Controls

Product Code FRG Wrap, Sterilization
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.6850
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 - FRG Wrap, Sterilization

All 122
Devices cleared under the same product code (FRG) and FDA review panel - the closest regulatory comparables to K801333.
GUARDIAN STERILIZATION WRAP
K803294 · Kimberly-Clark Corp. · Feb 1981
GUARDIAN PEEL POUCHES
K803293 · Kimberly-Clark Corp. · Jan 1981
HYPERALIMENTATION SUBCLAVIIAN DRESS TRAY
K802577 · Associated Medical Products Co. · Nov 1980
AMPCO HYPERALIMENTATION SUBCLAVIAN TRAYS
K801331 · Associated Medical Products Co. · Aug 1980
AMPCO SKIN SCRUB TRAYS
K801332 · Associated Medical Products Co. · Jun 1980
STERILIZER WRAP
K770514 · C.R. Bard, Inc. · Apr 1977