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

FQP 1978-10-17

SURGICAL LIGHT 22 SERIES

Applicant American Sterilizer Co.

K-Number K781581

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KYX 1978-10-17

PINT BOTTLE WELL

Applicant Baxa Corp., Sub. of Cook Group, Inc.

K-Number K781364

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ITY 1978-10-17

MAXIRAY 125 TUBE UNIT

Applicant General Electric Co.

K-Number K781524

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HFW 1978-10-17

UMBILICAL CORD CLAMP

Applicant Hollister, Inc.

K-Number K781548

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DJC 1978-10-17

KIDNEY, ARTIFICIAL

Applicant Bd Becton Dickinson Vacutainer Systems Preanalytic

K-Number K781153

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HJA 1978-10-17

TERRY KERATOMETER

Applicant Clifford M. Terry, M.C.

K-Number K781650

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IXQ 1978-10-17

PHIPIOLOGICAL SYNCHRONIZER PART#205

Applicant Brattle Instrument Corp.

K-Number K781681

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CEC 1978-10-17

RIA DIAG. TEST KIT FOR INDEXING THYROX.

Applicant Nuclear Diagnostics, Inc.

K-Number K781560

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GTZ 1978-10-17

STREP-TEX

Applicant Burroughs Wellcome Co.

K-Number K781607

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DXN 1978-10-17

PRESSURE INFUSION CUFF

Applicant Abbott Laboratories

K-Number K781556

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FHS 1978-10-17

DIALYZER, DISP., COIL, LUNDIA

Applicant Gambro, Inc.

K-Number K781102

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DRX 1978-10-17

ECG ELECTRODE, 2021, 2022, 2032, 2033

Applicant Cardio-Dynamics Laboratories, Inc.

K-Number K781514

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