510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K934174Substantially Equivalent

Ligaclip Endoscopic Rotating Multiple Clip Applier

Ethicon, Inc, Cincinnati OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K934174 is the FDA 510(k) clearance record for LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER, a class II device, cleared for ETHICON, Inc. on under FDA product code OCW (Endoscopic Tissue Approximation Device). FDA's definition for product code OCW reads: "To aid in endoscopically placing sutures, staples, clips, and other fastening tools through tissue". FDA records list 208 510(k) clearances for ETHICON, Inc., from to . As of , FDA records show no recalls naming K934174.

Clearance record

Decision date
Received
(194 days to decision)
Product code
OCW Endoscopic Tissue Approximation Device
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
ETHICON, Inc. 4545 Creek Rd., Cincinnati OH
510(k) summary
Summary
Third party review
No

Clearances, product code OCW

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