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FDA 510(k)

FINGERPRINT-DOA

K-Number: K942836 · 1995-05-01

ApplicantFingerprint Bioteck, Inc.
Decision Date1995-05-01
Product CodeDKZ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

FINGERPRINT-DOA is the device name listed in this FDA 510(k) record. The listed applicant is Fingerprint Bioteck, Inc.. It received FDA 510(k) clearance on 1995-05-01 under 510(k) number K942836. The device is classified under product code DKZ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FINGERPRINT-DOA?

FINGERPRINT-DOA is a medical device that received FDA 510(k) clearance on 1995-05-01. The listed applicant is Fingerprint Bioteck, Inc.. The 510(k) number is K942836.

When did FINGERPRINT-DOA receive FDA 510(k) clearance?

FINGERPRINT-DOA received FDA 510(k) clearance on 1995-05-01, under 510(k) number K942836.

Who is the listed applicant for FINGERPRINT-DOA?

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

What is the FDA product code for FINGERPRINT-DOA?

The FDA product code for FINGERPRINT-DOA is DKZ.

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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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