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FDA 510(k)

GS-7100 CHOLANGIOGRAM CLAMP, 5MM

K-Number: K900956 · 1990-04-18

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

Device Summary

GS-7100 CHOLANGIOGRAM CLAMP, 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 K900956. The device is classified under product code GDJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GS-7100 CHOLANGIOGRAM CLAMP, 5MM?

GS-7100 CHOLANGIOGRAM CLAMP, 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 K900956.

When did GS-7100 CHOLANGIOGRAM CLAMP, 5MM receive FDA 510(k) clearance?

GS-7100 CHOLANGIOGRAM CLAMP, 5MM received FDA 510(k) clearance on 1990-04-18, under 510(k) number K900956.

Who is the listed applicant for GS-7100 CHOLANGIOGRAM CLAMP, 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-7100 CHOLANGIOGRAM CLAMP, 5MM?

The FDA product code for GS-7100 CHOLANGIOGRAM CLAMP, 5MM is GDJ.

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: GDJ)

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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