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FDA 510(k)

CAOW HEMOSTASIS SYSTEM

K-Number: K972689 · 1998-08-27

ApplicantAnlam Corp.
Decision Date1998-08-27
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CAOW HEMOSTASIS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Anlam Corp.. It received FDA 510(k) clearance on 1998-08-27 under 510(k) number K972689. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAOW HEMOSTASIS SYSTEM?

CAOW HEMOSTASIS SYSTEM is a medical device that received FDA 510(k) clearance on 1998-08-27. The listed applicant is Anlam Corp.. The 510(k) number is K972689.

When did CAOW HEMOSTASIS SYSTEM receive FDA 510(k) clearance?

CAOW HEMOSTASIS SYSTEM received FDA 510(k) clearance on 1998-08-27, under 510(k) number K972689.

Who is the listed applicant for CAOW HEMOSTASIS SYSTEM?

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

What is the FDA product code for CAOW HEMOSTASIS SYSTEM?

The FDA product code for CAOW HEMOSTASIS SYSTEM is DXC.

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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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