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FDA 510(k)

ANGIO-BAND

K-Number: K923112 · 1992-09-23

ApplicantCook, Inc.
Decision Date1992-09-23
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ANGIO-BAND is the device name listed in this FDA 510(k) record. The listed applicant is Cook, Inc.. It received FDA 510(k) clearance on 1992-09-23 under 510(k) number K923112. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANGIO-BAND?

ANGIO-BAND is a medical device that received FDA 510(k) clearance on 1992-09-23. The listed applicant is Cook, Inc.. The 510(k) number is K923112.

When did ANGIO-BAND receive FDA 510(k) clearance?

ANGIO-BAND received FDA 510(k) clearance on 1992-09-23, under 510(k) number K923112.

Who is the listed applicant for ANGIO-BAND?

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

What is the FDA product code for ANGIO-BAND?

The FDA product code for ANGIO-BAND is IZI.

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Other records listing Cook, Inc. as applicant

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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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