FDA 510(k)

DAVIS+GECK VALTRAC BIOFRAG ANASTOMOSIS RING

K-Number: K931056 · 1993-07-08

Decision Date1993-07-08

Product CodeGDW

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

DAVIS+GECK VALTRAC BIOFRAG ANASTOMOSIS RING is the device name listed in this FDA 510(k) record. The listed applicant is American Cyanamid Co.. It received FDA 510(k) clearance on 1993-07-08 under 510(k) number K931056. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAVIS+GECK VALTRAC BIOFRAG ANASTOMOSIS RING?

DAVIS+GECK VALTRAC BIOFRAG ANASTOMOSIS RING is a medical device that received FDA 510(k) clearance on 1993-07-08. The listed applicant is American Cyanamid Co.. The 510(k) number is K931056.

When did DAVIS+GECK VALTRAC BIOFRAG ANASTOMOSIS RING receive FDA 510(k) clearance?

DAVIS+GECK VALTRAC BIOFRAG ANASTOMOSIS RING received FDA 510(k) clearance on 1993-07-08, under 510(k) number K931056.

Who is the listed applicant for DAVIS+GECK VALTRAC BIOFRAG ANASTOMOSIS RING?

The FDA 510(k) record lists American Cyanamid Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DAVIS+GECK VALTRAC BIOFRAG ANASTOMOSIS RING?

The FDA product code for DAVIS+GECK VALTRAC BIOFRAG ANASTOMOSIS RING is GDW.

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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.