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FDA 510(k)

DISPOSABLE GASTROINTESTINAL POLYPECTOMY SNARE

K-Number: K901428 · 1990-06-18

Decision Date1990-06-18
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE GASTROINTESTINAL POLYPECTOMY SNARE is the device name listed in this FDA 510(k) record. The listed applicant is Telemed Systems, Inc.. It received FDA 510(k) clearance on 1990-06-18 under 510(k) number K901428. The device is classified under product code FDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE GASTROINTESTINAL POLYPECTOMY SNARE?

DISPOSABLE GASTROINTESTINAL POLYPECTOMY SNARE is a medical device that received FDA 510(k) clearance on 1990-06-18. The listed applicant is Telemed Systems, Inc.. The 510(k) number is K901428.

When did DISPOSABLE GASTROINTESTINAL POLYPECTOMY SNARE receive FDA 510(k) clearance?

DISPOSABLE GASTROINTESTINAL POLYPECTOMY SNARE received FDA 510(k) clearance on 1990-06-18, under 510(k) number K901428.

Who is the listed applicant for DISPOSABLE GASTROINTESTINAL POLYPECTOMY SNARE?

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

What is the FDA product code for DISPOSABLE GASTROINTESTINAL POLYPECTOMY SNARE?

The FDA product code for DISPOSABLE GASTROINTESTINAL POLYPECTOMY SNARE is FDI.

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 Telemed Systems, 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 22 devices →

Related Devices (Code: FDI)

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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