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

KYA 1982-04-29

PARATHERM

Applicant American Thermometer Company, Inc.

K-Number K821049

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IMD 1982-04-29

COMPRES PORTABLE HEAT PADS

Applicant S.C. Johnson & Son, Inc.

K-Number K821046

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FRN 1982-04-29

AS 70 VOLUMETRIC INFUSION PUMP

Applicant Narco Scientific

K-Number K820946

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KNT 1982-04-29

VIVONEX ACUTROL ENTERNAL FEEDING SYS

Applicant Norwich Eaton Pharmaceuticals, Inc.

K-Number K821067

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GZJ 1982-04-29

MODEL 860-1 VERI/PROBE

Applicant Verite

K-Number K820651

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DYG 1982-04-29

SEPTISLEEVE

Applicant Argon Medical Corp.

K-Number K820883

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DEW 1982-04-29

ANTIHUMAN IGG GLOBULIN FITC LABELED

Applicant Microbiological Research Corp.

K-Number K821018

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JHI 1982-04-29

TANDEM HCG KIT

Applicant Hybritech, Inc.

K-Number K820822

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DXC 1982-04-29

P-S BERLIN VESSEL CLAMP

Applicant Pudenz-Schulte Medical Research Corp.

K-Number K820949

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GZJ 1982-04-29

BIGSTON TRANSCUTANEOUS NERVE STIMULAT

Applicant Canadian Medical Products

K-Number K820326

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DWJ 1982-04-29

THERMO-K

Applicant American Medical Systems, Inc.

K-Number K820814

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DXG 1982-04-29

CARDIO REVUE CENTER

Applicant Diasonics, Inc.

K-Number K820820

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