FDA 510(k)

AWC BUTTERFLY WOUND CLOSURES

K-Number: K894802 · 1990-01-31

Decision Date1990-01-31

Product CodeFPX

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

AWC BUTTERFLY WOUND CLOSURES is the device name listed in this FDA 510(k) record. The listed applicant is American White Cross, Inc.. It received FDA 510(k) clearance on 1990-01-31 under 510(k) number K894802. The device is classified under product code FPX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AWC BUTTERFLY WOUND CLOSURES?

AWC BUTTERFLY WOUND CLOSURES is a medical device that received FDA 510(k) clearance on 1990-01-31. The listed applicant is American White Cross, Inc.. The 510(k) number is K894802.

When did AWC BUTTERFLY WOUND CLOSURES receive FDA 510(k) clearance?

AWC BUTTERFLY WOUND CLOSURES received FDA 510(k) clearance on 1990-01-31, under 510(k) number K894802.

Who is the listed applicant for AWC BUTTERFLY WOUND CLOSURES?

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

What is the FDA product code for AWC BUTTERFLY WOUND CLOSURES?

The FDA product code for AWC BUTTERFLY WOUND CLOSURES is FPX.

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Other records listing American White Cross, Inc. as applicant

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Related Devices (Code: FPX)

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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.