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FDA 510(k)

GS-5200 HOOK SUCTION/COAGULATOR, 5MM

K-Number: K900954 · 1990-04-18

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

Device Summary

GS-5200 HOOK SUCTION/COAGULATOR, 5MM 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 K900954. 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 GS-5200 HOOK SUCTION/COAGULATOR, 5MM?

GS-5200 HOOK SUCTION/COAGULATOR, 5MM 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 K900954.

When did GS-5200 HOOK SUCTION/COAGULATOR, 5MM receive FDA 510(k) clearance?

GS-5200 HOOK SUCTION/COAGULATOR, 5MM received FDA 510(k) clearance on 1990-04-18, under 510(k) number K900954.

Who is the listed applicant for GS-5200 HOOK SUCTION/COAGULATOR, 5MM?

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-5200 HOOK SUCTION/COAGULATOR, 5MM?

The FDA product code for GS-5200 HOOK SUCTION/COAGULATOR, 5MM is GEI.

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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 KITK900956GS-7100 CHOLANGIOGRAM CLAMP, 5MMK900964CANNULA AND TROCAR, 11MMK900949GS-1100 MICRO DISSECTING FORCEP, 5MM, INSULATEDK900955GS-4000 REDUCER SLEEVE, 11MM TO 5MM

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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.

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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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