STAINLESS STEEL, GUT, POLY (GLYCOLIDE/L-LACTIDE) POLYAMIDE, POLYPROPYLENE, POLY (ETHYLENE TEREPHTHALATE) AND SILK— 510(k) K946173

Substantially Equivalent

ETHICON, Inc.

FDA 510(k) clearance K946173 for STAINLESS STEEL, GUT, POLY (GLYCOLIDE/L-LACTIDE) POLYAMIDE, POLYPROPYLENE, POLY (ETHYLENE TEREPHTHALATE) AND SILK, Substantially Equivalent on 1995-01-09. Applicant: ETHICON, Inc.. Device class: 2.

Clearance details

Applicant
ETHICON, Inc.
Product code
Code GAQ
Device class
Class 2
Regulation
21 CFR 878.4495
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Somerville, NJ, US
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Adverse events under product code GAQ

product code GAQ
Death
3
Malfunction
522
Total
525

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recalls naming K946173

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K946173.

Data sourced from openFDA. This site is unofficial and independent of the FDA.