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FDA 510(k)

ABUSIGN DOA4

K-Number: K943439 · 1995-02-22

ApplicantPrinceton BioMeditech Corp.
Decision Date1995-02-22
Product CodeDKZ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

ABUSIGN DOA4 is the device name listed in this FDA 510(k) record. The listed applicant is Princeton BioMeditech Corp.. It received FDA 510(k) clearance on 1995-02-22 under 510(k) number K943439. 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 ABUSIGN DOA4?

ABUSIGN DOA4 is a medical device that received FDA 510(k) clearance on 1995-02-22. The listed applicant is Princeton BioMeditech Corp.. The 510(k) number is K943439.

When did ABUSIGN DOA4 receive FDA 510(k) clearance?

ABUSIGN DOA4 received FDA 510(k) clearance on 1995-02-22, under 510(k) number K943439.

Who is the listed applicant for ABUSIGN DOA4?

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

What is the FDA product code for ABUSIGN DOA4?

The FDA product code for ABUSIGN DOA4 is DKZ.

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Other records listing Princeton BioMeditech Corp. as applicant

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Related Devices (Code: DKZ)

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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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