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FDA 510(k)

GS-1002 GRASPING FORCEP, 5MM WITH RATCHET

K-Number: K900948 · 1990-04-18

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

Device Summary

GS-1002 GRASPING FORCEP, 5MM WITH RATCHET 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 K900948. 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-1002 GRASPING FORCEP, 5MM WITH RATCHET?

GS-1002 GRASPING FORCEP, 5MM WITH RATCHET 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 K900948.

When did GS-1002 GRASPING FORCEP, 5MM WITH RATCHET receive FDA 510(k) clearance?

GS-1002 GRASPING FORCEP, 5MM WITH RATCHET received FDA 510(k) clearance on 1990-04-18, under 510(k) number K900948.

Who is the listed applicant for GS-1002 GRASPING FORCEP, 5MM WITH RATCHET?

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-1002 GRASPING FORCEP, 5MM WITH RATCHET?

The FDA product code for GS-1002 GRASPING FORCEP, 5MM WITH RATCHET is GEN.

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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 KITK900954GS-5200 HOOK SUCTION/COAGULATOR, 5MMK900964CANNULA AND TROCAR, 11MMK900949GS-1100 MICRO DISSECTING FORCEP, 5MM, INSULATEDK900955GS-4000 REDUCER SLEEVE, 11MM TO 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.K900951GS-7000 CLIP-APPLYING FORCEP, 10MM, MEDIUM CLIPSolos 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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