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FDA 510(k)

GS-7000 CLIP-APPLYING FORCEP, 10MM, MEDIUM CLIP

K-Number: K900951 · 1990-04-18

ApplicantSolos Endoscopy, Inc.
Decision Date1990-04-18
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GS-7000 CLIP-APPLYING FORCEP, 10MM, MEDIUM CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Solos Endoscopy, Inc.. It received FDA 510(k) clearance on 1990-04-18 under 510(k) number K900951. The device is classified under product code GEN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GS-7000 CLIP-APPLYING FORCEP, 10MM, MEDIUM CLIP?

GS-7000 CLIP-APPLYING FORCEP, 10MM, MEDIUM CLIP is a medical device that received FDA 510(k) clearance on 1990-04-18. The listed applicant is Solos Endoscopy, Inc.. The 510(k) number is K900951.

When did GS-7000 CLIP-APPLYING FORCEP, 10MM, MEDIUM CLIP receive FDA 510(k) clearance?

GS-7000 CLIP-APPLYING FORCEP, 10MM, MEDIUM CLIP received FDA 510(k) clearance on 1990-04-18, under 510(k) number K900951.

Who is the listed applicant for GS-7000 CLIP-APPLYING FORCEP, 10MM, MEDIUM CLIP?

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

What is the FDA product code for GS-7000 CLIP-APPLYING FORCEP, 10MM, MEDIUM CLIP?

The FDA product code for GS-7000 CLIP-APPLYING FORCEP, 10MM, MEDIUM CLIP is GEN.

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 Solos Endoscopy, Inc. 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.

K983538MINIATURIZED BIOPSY,SCOPE A.K.A: BIOPSY NEEDLE WITH ENDOSCOPIC VIEWING CAPABILITYK910671MODEL GS-4700 COMMON DUCT STONE REMOVING KITK900956GS-7100 CHOLANGIOGRAM CLAMP, 5MMK900955GS-4000 REDUCER SLEEVE, 11MM TO 5MMK900964CANNULA AND TROCAR, 11MMK900954GS-5200 HOOK SUCTION/COAGULATOR, 5MM

View all 21 devices →

Related Devices (Code: GEN)

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.

K031828NATURALASE LP ND:YAG LASERFocus Medical, LLCK953962FORCEPSBiopsys Medical, Inc.K932385SUTURE REMOVING FORCEPSRocket of London, Ltd.K904723FORCEPSMinto Research & Development, Inc.K911159PALPATION PROBENorthgate Technologies, Inc.K900952GS-1200 GRASPING/EXTRACTING FORCEP, 10MMSolos Endoscopy, Inc.

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.

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