Cleared Traditional

K792630 - STERILIZATION PROCESS/X-RAY DETECT. SPG

K792630 is the FDA 510(k) clearance for STERILIZATION PROCESS/X-RAY DETECT. SPG by Procter & Gamble Mfg. Co.. It is a Class 1 General & Plastic Surgery device (product code GDY) cleared through the Traditional 510(k) pathway after a 23-day FDA review.

K792630 · Procter & Gamble Mfg. Co. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 1980
Decision
23d
Days
Class 1
Risk

K792630 is an FDA 510(k) clearance for the STERILIZATION PROCESS/X-RAY DETECT. SPG. Classified as Gauze/sponge, Internal, X-ray Detectable (product code GDY), Class I - General Controls.

Submitted by Procter & Gamble Mfg. Co. (Mchenry, US). The FDA issued a Cleared decision on January 11, 1980 after a review of 23 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4450 - the FDA general and plastic surgery 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 Procter & Gamble Mfg. Co. devices

Submission Details

510(k) Number K792630 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 19, 1979
Decision Date January 11, 1980
Days to Decision 23 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
92d faster than avg
Panel avg: 115d · This submission: 23d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code GDY Gauze/sponge, Internal, X-ray Detectable
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4450
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 - GDY Gauze/sponge, Internal, X-ray Detectable

All 7
Devices cleared under the same product code (GDY) and FDA review panel - the closest regulatory comparables to K792630.
QUALTEX NEUROLOK SURGICAL SPONGE
K884790 · Deroyal Industries, Inc. · Dec 1988
X-RAY DETECTABLE LAP SPONGES
K812651 · Procter & Gamble Mfg. Co. · Oct 1981
GAUZE SPONGES
K803188 · Abco Dealers, Inc. · Jan 1981
SOF-WICKLAP PAD
K780718 · Johnson & Johnson Professionals, Inc. · Jun 1978
LAPAROTOMY SPONGES, STERILE
K771395 · Medline Industries, Inc. · Aug 1977