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FDA 510(k)

LIFESIGN COC, STATUS STIK COC, ACCUSIGN STIK COC, ACCUSTIK COC

K-Number: K014069 · 2002-06-10

ApplicantPrinceton BioMeditech Corp.
Decision Date2002-06-10
Product CodeDIO
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

LIFESIGN COC, STATUS STIK COC, ACCUSIGN STIK COC, ACCUSTIK COC 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 2002-06-10 under 510(k) number K014069. The device is classified under product code DIO. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFESIGN COC, STATUS STIK COC, ACCUSIGN STIK COC, ACCUSTIK COC?

LIFESIGN COC, STATUS STIK COC, ACCUSIGN STIK COC, ACCUSTIK COC is a medical device that received FDA 510(k) clearance on 2002-06-10. The listed applicant is Princeton BioMeditech Corp.. The 510(k) number is K014069.

When did LIFESIGN COC, STATUS STIK COC, ACCUSIGN STIK COC, ACCUSTIK COC receive FDA 510(k) clearance?

LIFESIGN COC, STATUS STIK COC, ACCUSIGN STIK COC, ACCUSTIK COC received FDA 510(k) clearance on 2002-06-10, under 510(k) number K014069.

Who is the listed applicant for LIFESIGN COC, STATUS STIK COC, ACCUSIGN STIK COC, ACCUSTIK COC?

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 LIFESIGN COC, STATUS STIK COC, ACCUSIGN STIK COC, ACCUSTIK COC?

The FDA product code for LIFESIGN COC, STATUS STIK COC, ACCUSIGN STIK COC, ACCUSTIK COC is DIO.

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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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