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FDA 510(k)

TI-CRON AND DACRON SUTURES

K-Number: K930591 · 1993-12-17

ApplicantDavis & Geck, Inc.
Decision Date1993-12-17
Product CodeGAT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TI-CRON AND DACRON SUTURES 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 K930591. The device is classified under product code GAT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TI-CRON AND DACRON SUTURES?

TI-CRON AND DACRON SUTURES 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 K930591.

When did TI-CRON AND DACRON SUTURES receive FDA 510(k) clearance?

TI-CRON AND DACRON SUTURES received FDA 510(k) clearance on 1993-12-17, under 510(k) number K930591.

Who is the listed applicant for TI-CRON AND DACRON SUTURES?

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 TI-CRON AND DACRON SUTURES?

The FDA product code for TI-CRON AND DACRON SUTURES is GAT.

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Other records listing Davis & Geck, Inc. as applicant

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Related Devices (Code: GAT)

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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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