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FDA 510(k)

GS-2100 HOOK SUTURE SCISSOR, 5MM

K-Number: K900957 · 1990-04-18

Decision Date1990-04-18
Product CodeLRW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GS-2100 HOOK SUTURE SCISSOR, 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 K900957. The device is classified under product code LRW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GS-2100 HOOK SUTURE SCISSOR, 5MM?

GS-2100 HOOK SUTURE SCISSOR, 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 K900957.

When did GS-2100 HOOK SUTURE SCISSOR, 5MM receive FDA 510(k) clearance?

GS-2100 HOOK SUTURE SCISSOR, 5MM received FDA 510(k) clearance on 1990-04-18, under 510(k) number K900957.

Who is the listed applicant for GS-2100 HOOK SUTURE SCISSOR, 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-2100 HOOK SUTURE SCISSOR, 5MM?

The FDA product code for GS-2100 HOOK SUTURE SCISSOR, 5MM is LRW.

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.

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.

View all 21 devices →

Related Devices (Code: LRW)

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.

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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