510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K914588Substantially Equivalent

Grieshaber Snare Instrument and Snare Cartridge

Grieshaber & Co., Langhorne PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K914588 is the FDA 510(k) clearance record for GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGE, a class II device, cleared for Grieshaber & Co. on under FDA product code GAW (Suture, Nonabsorbable, Synthetic, Polypropylene). FDA records list 15 510(k) clearances for Grieshaber & Co., from to . As of , FDA records show no recalls naming K914588.

Clearance record

Decision date
Received
(239 days to decision)
Product code
GAW Suture, Nonabsorbable, Synthetic, Polypropylene
Regulation
21 CFR 878.5010
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Grieshaber & Co. 3000 Cabot Blvd. W., Langhorne PA
510(k) summary
Statement
Third party review
No

Clearances, product code GAW

Trailing 12 months
1 clearance under product code GAW in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code GAW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260