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FDA 510(k)

CLP ABNORMAL COAGULATION CONTROL

K-Number: K881510 · 1988-05-06

ApplicantCreative Laboratory Products, Inc.
Decision Date1988-05-06
Product CodeGGC
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

CLP ABNORMAL COAGULATION CONTROL 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 1988-05-06 under 510(k) number K881510. The device is classified under product code GGC. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLP ABNORMAL COAGULATION CONTROL?

CLP ABNORMAL COAGULATION CONTROL is a medical device that received FDA 510(k) clearance on 1988-05-06. The listed applicant is Creative Laboratory Products, Inc.. The 510(k) number is K881510.

When did CLP ABNORMAL COAGULATION CONTROL receive FDA 510(k) clearance?

CLP ABNORMAL COAGULATION CONTROL received FDA 510(k) clearance on 1988-05-06, under 510(k) number K881510.

Who is the listed applicant for CLP ABNORMAL COAGULATION CONTROL?

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 ABNORMAL COAGULATION CONTROL?

The FDA product code for CLP ABNORMAL COAGULATION CONTROL is GGC.

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Other records listing Creative Laboratory Products, Inc. as applicant

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Related Devices (Code: GGC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K102552HEMOSIL LA POSITIVE CONTROLInstrumentation Laboratory COK100103SPECIALTY ASSAYED CONTROL-2Helena LaboratoriesK062306PLASMACON N, PLASMACON L-1, PLASMACON L-2R2 Diagnostics, Inc.K061803STA - CONTROL LA 1+2Diagnostica Stago, Inc.K032804CRYOCHECK WEAK LUPUS POSITIVE CONTROLPrecision BiologicK023312CONTROL PLASMA PDade Behring, Inc.

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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