FDA 510(k)

STORZ S2050 SERIES BIPOLAR FORCEPS

K-Number: K960009 · 1996-03-06

Decision Date1996-03-06

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

STORZ S2050 SERIES BIPOLAR FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Storz Instrument Co.. It received FDA 510(k) clearance on 1996-03-06 under 510(k) number K960009. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STORZ S2050 SERIES BIPOLAR FORCEPS?

STORZ S2050 SERIES BIPOLAR FORCEPS is a medical device that received FDA 510(k) clearance on 1996-03-06. The listed applicant is Storz Instrument Co.. The 510(k) number is K960009.

When did STORZ S2050 SERIES BIPOLAR FORCEPS receive FDA 510(k) clearance?

STORZ S2050 SERIES BIPOLAR FORCEPS received FDA 510(k) clearance on 1996-03-06, under 510(k) number K960009.

Who is the listed applicant for STORZ S2050 SERIES BIPOLAR FORCEPS?

The FDA 510(k) record lists Storz Instrument Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STORZ S2050 SERIES BIPOLAR FORCEPS?

The FDA product code for STORZ S2050 SERIES BIPOLAR FORCEPS is GEI.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Storz Instrument Co. as applicant

K980100STORZ DP4210 VENTURI ECONOMY ANTERIOR PACK AND DP5000 ASC DAYPACK K980488STORZ MILLENNIUM MICROSURGICL SYSTEM HIGH SPEED VITRECTOMY SYSTEM K972664STORZ MILLENNIUM VISCOUS FLUID SYSTEM K971439STORZ MICROFLOW AND STORZ STANDARD PHACOEMULSIFICATION NEEDLES K964743STORZ E8010 ERGOTEC/PREMIERE ADAPTOR K960024STORZ D7120 PHACO HANDPIECE MAINTENANCE KIT & STORZ D7125 PHACO HANDPIECE NEEDLE WRENCH

View all 101 devices →

Related Devices (Code: GEI)

K261959Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Push Button Switch (0703-046-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Push Button Switch, Bulk Non-Sterile (0703-046-102);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Rocker Switch (0703-047-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Rocker Switch, Bulk Non-Sterile (0703-047-102)Stryker Instruments K254196HARMONIC 1100 Shears (HAR1120); HARMONIC 1100 Shears (HAR1136)Ethicon Endo-Surgery, LLC K261070LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coatedCovidien, LLC K254185Potenza PrimeJeisys Medical Incorporated K262364Ellian Enigma RF DeviceEllian Corp K253859Scarlet Pro (Scarlet Pro)VIOL Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.