510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K970968Substantially Equivalent

Bissinger Detachable Bipolar Coagulation-Forceps

Guenter Bissinger Medizintechnik GmbH, Teningen, DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K970968 is the FDA 510(k) clearance record for BISSINGER DETACHABLE BIPOLAR COAGULATION-FORCEPS, a class II device, cleared for Guenter Bissinger Medizintechnik GmbH on under FDA product code HET (Laparoscope, Gynecologic (And Accessories)). FDA records list 6 510(k) clearances for Guenter Bissinger Medizintechnik GmbH, from to . As of , FDA records show no recalls naming K970968.

Clearance record

Decision date
Received
(430 days to decision)
Product code
HET Laparoscope, Gynecologic (And Accessories)
Regulation
21 CFR 884.1720
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Guenter Bissinger Medizintechnik GmbH Gottlieb-Daimler-Str. 5, Teningen, DE
510(k) summary
Summary
Third party review
No

Clearances, product code HET

Trailing 12 months

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

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