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FDA 510(k)

CLP NORMAL COAGULATION CONTROL

K-Number: K880712 · 1988-05-06

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

Device Summary

CLP NORMAL 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 K880712. The device is classified under product code GIZ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLP NORMAL COAGULATION CONTROL?

CLP NORMAL 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 K880712.

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

CLP NORMAL COAGULATION CONTROL received FDA 510(k) clearance on 1988-05-06, under 510(k) number K880712.

Who is the listed applicant for CLP NORMAL 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 NORMAL COAGULATION CONTROL?

The FDA product code for CLP NORMAL COAGULATION CONTROL is GIZ.

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Other records listing Creative Laboratory Products, Inc. as applicant

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.

K950589CLP HIGH LEVEL HIGH DENSITY LIPO PROTEIN CHOLESTEROL CONTROL-HLK942284CLP TOTAL IRON AND UIBC/TIBC LINEARITY CONTROL SETK922995LIPID CONTROLSK913427SICKLE HEMOGLOBIN (HBA/S) CONTROL SETK913371TOTAL IRON AND UNSAT IRON BIND CAPAC/IRON BIND CALK913585LIPASE LINEARITY CONTROL

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Related Devices (Code: GIZ)

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.

K060968STASIS - I, II AND III; SERATHAN - A, B; INTRIN - EA, SI CALCIUM CHLORIDE 0.02M; FIBRINOGEN CONTROL-NORMAL, LOWWortham Laboratories, Inc.K042941DADE BEHRING HEPARIN CALIBRATOR AND CONTROLSDade Behring, Inc.K023309CONTROL PLASMA NDade Behring, Inc.K013708REFERENCE CHECK, CATALOG NUMBER-RCN-10Precision BiologicK003328ACCUCLOT CONTROL I, MODEL A4089Sigma Diagnostics, Inc.K001256CONTROL PLASMA NDade 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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