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

JQW 1980-06-09

J.T. BAKER LSA 290 PIPETTER/DILUTER

Applicant J.T. Baker Chemical Co.

K-Number K801090

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CDP 1980-06-09

SPAC T3 RIA TEST KIT

Applicant Mallinckrodt Critical Care

K-Number K801125

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CAP 1980-06-09

PENLON I.D.P. PRESSSURE FAILURE ALARM

Applicant Penlon, Inc.

K-Number K801254

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KDQ 1980-06-09

THORA-DRAIN III PLASTIC DRAINAGE SYSTEM

Applicant Chesebrough-Pond'S U.S.A. Co.

K-Number K801221

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DXQ 1980-06-09

CONPHAR DELUXE ANEROID SPHYGMOMANOMETER

Applicant Conphar, Inc.

K-Number K801186

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MMK 1980-06-09

NEEDLE COUNTER-SURE COUNT/100 COUNT

Applicant Kleen Test Products

K-Number K801259

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CIG 1980-06-09

COBAS TOTAL BILIRUBIN REAGENT & DILUENT

Applicant Roche Analytical Instruments, Inc.

K-Number K801117

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GGW 1980-06-04

A-GENT QUANTICHROM THROMBIGEN I

Applicant Abbott Laboratories

K-Number K800725

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EMA 1980-06-04

BONDALCAP (SILICO-PHOSPHATE)

Applicant Vivadent (Usa), Inc.

K-Number K801228

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DTB 1980-06-04

LIFELINE TLE J-SHAPED ATRIAL ENDOCARDIAL

Applicant Intermedics, Inc.

K-Number K792301

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LDE 1980-06-04

ABCO PEDIATRIC STETHOSCOPE

Applicant Abco Dealers, Inc.

K-Number K801215

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FXX 1980-06-04

SURGICAL MASK

Applicant American Threshold Industries, Inc.

K-Number K801036

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