Cleared Traditional

K802375 - AMPCO SKIN SCRUB TRAY

K802375 is an FDA 510(k) clearance for AMPCO SKIN SCRUB TRAY, manufactured by Associated Medical Products Co.. The device is a Class 1 General Hospital device with product code FMC cleared through the Traditional 510(k) pathway after a 10-day FDA review.

K802375 · Associated Medical Products Co. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 1980
Decision
10d
Days
Class 1
Risk

K802375 is an FDA 510(k) clearance for the AMPCO SKIN SCRUB TRAY. Classified as Patient Examination Glove (product code FMC), Class I - General Controls.

Submitted by Associated Medical Products Co. (Mchenry, US). The FDA issued a Cleared decision on October 10, 1980 after a review of 10 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6250 - 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 - K802375

510(k) Number K802375 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 30, 1980
Decision Date October 10, 1980
Days to Decision 10 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
119d faster than avg
Panel avg: 129d · This submission: 10d
Pathway characteristics
Predicate-based equivalence.

FMC Device Classification - Class 1, General Controls

Product Code FMC Patient Examination Glove
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6250
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 - FMC Patient Examination Glove

All 9
Devices cleared under the same product code (FMC) and FDA review panel - the closest regulatory comparables to K802375.
ORTHOPEDIC SURGICAL GLOVE
K831564 · Ansell, Inc. · Jul 1983
FINGER COTS
K821028 · Abco Dealers, Inc. · Apr 1982
SUTURE WOUND TRAY MILFORD WHITTINSVILLE
K802386 · American Medical Disposable, Inc. · Nov 1980
EMBOSSED DISP. POLY. GLOVES #5101-03
K801997 · Pollak (Intl.), Ltd. · Sep 1980
STERILE EXAMINATION GLOVE #5121-5126
K801998 · Pollak (Intl.), Ltd. · Sep 1980
CONPHAR EXAM. GLOVES, POLYETHYLENE
K791805 · Conphar, Inc. · Oct 1979