510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K940661Substantially Equivalent

Stiegmann-Goff Endoscopic Ligator

C.R. Bard Inc, Tewksbury MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K940661 is the FDA 510(k) clearance record for STIEGMANN-GOFF ENDOSCOPIC LIGATOR, a class II device, cleared for C.R. Bard, Inc. on under FDA product code MND (Ligator, Esophageal). FDA records list 646 510(k) clearances for C.R. Bard, Inc., from to . As of , FDA records show no recalls naming K940661.

Clearance record

Decision date
Received
(286 days to decision)
Product code
MND Ligator, Esophageal
Regulation
21 CFR 876.4400
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
C.R. Bard, Inc. 200 Ames Pond Dr., Tewksbury MA
510(k) summary
Summary
Third party review
No

Clearances, product code MND

Trailing 12 months

FDA records hold no clearances under product code MND in the trailing twelve months.

FDA records show no clearances under product code MND in the twelve months to November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MND, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260