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FDA 510(k)

PLAIN, MILD CHROMIC AND CHROMIC SURGICAL GUT SUTUR

K-Number: K930589 · 1993-12-17

Decision Date1993-12-17
Product CodeGAL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PLAIN, MILD CHROMIC AND CHROMIC SURGICAL GUT SUTUR is the device name listed in this FDA 510(k) record. The listed applicant is Davis & Geck, Inc.. It received FDA 510(k) clearance on 1993-12-17 under 510(k) number K930589. The device is classified under product code GAL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLAIN, MILD CHROMIC AND CHROMIC SURGICAL GUT SUTUR?

PLAIN, MILD CHROMIC AND CHROMIC SURGICAL GUT SUTUR is a medical device that received FDA 510(k) clearance on 1993-12-17. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K930589.

When did PLAIN, MILD CHROMIC AND CHROMIC SURGICAL GUT SUTUR receive FDA 510(k) clearance?

PLAIN, MILD CHROMIC AND CHROMIC SURGICAL GUT SUTUR received FDA 510(k) clearance on 1993-12-17, under 510(k) number K930589.

Who is the listed applicant for PLAIN, MILD CHROMIC AND CHROMIC SURGICAL GUT SUTUR?

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

What is the FDA product code for PLAIN, MILD CHROMIC AND CHROMIC SURGICAL GUT SUTUR?

The FDA product code for PLAIN, MILD CHROMIC AND CHROMIC SURGICAL GUT SUTUR is GAL.

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 Davis & Geck, 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 45 devices →

Related Devices (Code: GAL)

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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