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FDA 510(k)

ENDOSCOPIC SCISSORS (DISPOSABLE/REUSABLE SHAFTS)

K-Number: K926203 · 1993-10-15

ApplicantWeck Endoscopy
Decision Date1993-10-15
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPIC SCISSORS (DISPOSABLE/REUSABLE SHAFTS) is the device name listed in this FDA 510(k) record. The listed applicant is Weck Endoscopy. It received FDA 510(k) clearance on 1993-10-15 under 510(k) number K926203. 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 ENDOSCOPIC SCISSORS (DISPOSABLE/REUSABLE SHAFTS)?

ENDOSCOPIC SCISSORS (DISPOSABLE/REUSABLE SHAFTS) is a medical device that received FDA 510(k) clearance on 1993-10-15. The listed applicant is Weck Endoscopy. The 510(k) number is K926203.

When did ENDOSCOPIC SCISSORS (DISPOSABLE/REUSABLE SHAFTS) receive FDA 510(k) clearance?

ENDOSCOPIC SCISSORS (DISPOSABLE/REUSABLE SHAFTS) received FDA 510(k) clearance on 1993-10-15, under 510(k) number K926203.

Who is the listed applicant for ENDOSCOPIC SCISSORS (DISPOSABLE/REUSABLE SHAFTS)?

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

What is the FDA product code for ENDOSCOPIC SCISSORS (DISPOSABLE/REUSABLE SHAFTS)?

The FDA product code for ENDOSCOPIC SCISSORS (DISPOSABLE/REUSABLE SHAFTS) 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_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Weck Endoscopy as applicant

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.

K930550ECO LIGATING CLIPK926223ENDOSCOPE AND ACCESSORIESK930082ENDOSCOPE AND ACCESSORIES

Related Devices (Code: GEI)

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.

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 InstrumentsK254196HARMONIC 1100 Shears (HAR1120); HARMONIC 1100 Shears (HAR1136)Ethicon Endo-Surgery, LLCK261070LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coatedCovidien, LLCK254185Potenza PrimeJeisys Medical IncorporatedK262364Ellian Enigma RF DeviceEllian CorpK253859Scarlet Pro (Scarlet Pro)VIOL Co., Ltd.

Official Source

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

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