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

JBX 1978-10-24

BUFFER, COLLAGEN REAGENT AND DILUENT

Applicant Diagnostica, Inc.

K-Number K781710

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KGC 1978-10-24

CENTRAL CATHETER TRAY

Applicant Argon Medical Corp.

K-Number K781333

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KCT 1978-10-24

EAGLE PAC/VISIBLE SEAL

Applicant American Sterilizer Co.

K-Number K781699

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DON 1978-10-24

RIA, DIGOXIN

Applicant E. R. Squibb & Sons, Inc.

K-Number K781660

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DJC 1978-10-24

DIALYSIS SYS., PDS 400 & RO 400

Applicant Physio-Control Corp.

K-Number K781156

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HLT 1978-10-24

ORBIOGRAPH

Applicant Sonometrics Systems, Inc.

K-Number K781543

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GEX 1978-10-24

MODEL 770 ARGON LASER

Applicant Spectra-Physics, Inc.

K-Number K781453

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CJE 1978-10-24

ALKALINE PHOSPHATASE IN SERUM

Applicant Fisher Scientific Co., LLC

K-Number K781609

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GEI 1978-10-24

DISPOSABLE LECTROSWITCH, MODEL E2503

Applicant Valleylab, Inc.

K-Number K781510

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GOK 1978-10-24

CYTOMEGILISH TEST KIT

Applicant Microbiological Assoc.

K-Number K781392

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IZL 1978-10-24

MOBIL XR

Applicant Siemens Corp.

K-Number K781705

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IYO 1978-10-24

SCANNER, LINEAR

Applicant Philips Medical Systems (Cleveland), Inc.

K-Number K781709

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