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FDA 510(k)

CLP ACTIVATED PARTIAL THROMBOPLASTIN TIME TEST

K-Number: K881068 · 1988-03-23

ApplicantCreative Laboratory Products, Inc.
Decision Date1988-03-23
Product CodeGFO
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

CLP ACTIVATED PARTIAL THROMBOPLASTIN TIME TEST is the device name listed in this FDA 510(k) record. The listed applicant is Creative Laboratory Products, Inc.. It received FDA 510(k) clearance on 1988-03-23 under 510(k) number K881068. The device is classified under product code GFO. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLP ACTIVATED PARTIAL THROMBOPLASTIN TIME TEST?

CLP ACTIVATED PARTIAL THROMBOPLASTIN TIME TEST is a medical device that received FDA 510(k) clearance on 1988-03-23. The listed applicant is Creative Laboratory Products, Inc.. The 510(k) number is K881068.

When did CLP ACTIVATED PARTIAL THROMBOPLASTIN TIME TEST receive FDA 510(k) clearance?

CLP ACTIVATED PARTIAL THROMBOPLASTIN TIME TEST received FDA 510(k) clearance on 1988-03-23, under 510(k) number K881068.

Who is the listed applicant for CLP ACTIVATED PARTIAL THROMBOPLASTIN TIME TEST?

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

What is the FDA product code for CLP ACTIVATED PARTIAL THROMBOPLASTIN TIME TEST?

The FDA product code for CLP ACTIVATED PARTIAL THROMBOPLASTIN TIME TEST is GFO.

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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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