Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k) Clearances

510(k) cleared devices tracked by MedTracker

CFE 1979-10-01

LDH CLINI GEL KIT

Applicant Clinical Sciences, Inc.

K-Number K791827

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FRN 1979-10-01

SYRINGE INFUSION PUMP

Applicant Princeton Medical Instruments, Inc.

K-Number K791729

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JSJ 1979-10-01

SABOURAUD AGAR MODIFIED

Applicant Isle Media and Sterile Products, Inc.

K-Number K791670

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JSG 1979-10-01

CDC ANAEROBIC SHEEP BLOOD AGAR (BA)

Applicant Gibco Laboratories Life Technologies, Inc.

K-Number K791698

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KPE 1979-10-01

ADDITIVE HINGE CAP

Applicant Abbott Laboratories

K-Number K791796

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JHT 1979-10-01

CPK CLINI GEL KIT

Applicant Clinical Sciences, Inc.

K-Number K791826

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CGA 1979-10-01

GLUCOSE OXIDASE (FRINDER) KIT

Applicant Mid Tech, Inc.

K-Number K791869

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FDX 1979-10-01

ENDOSCOPIC CYTOLOGY BRUSHES

Applicant Mill-Rose Laboratory

K-Number K791668

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JMF 1979-10-01

CENTRIA HPL RIA

Applicant Union Carbide Corp.

K-Number K791854

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ILZ 1979-10-01

CERVI-TRAC

Applicant Dr. K.G. Rude

K-Number K791808

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CGJ 1979-10-01

QUANTIMUNE HFSH RIA

Applicant Bio-Rad

K-Number K791836

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DSP 1979-10-01

INTRA-AORTIC BALLOON, TYPE S

Applicant Datascope Corp.

K-Number K790775

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