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

N/A 1982-09-29

ADR ULTRASOUND MODEL 4000 SC OR 4000 S/LC

Applicant Adr Ultrasound

K-Number K828051

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N/A 1982-09-29

ADR ULTRASOUND 5.5 MHZ SHORT FOCUS TRANSDUCER

Applicant Adr Ultrasound

K-Number K828053

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N/A 1982-09-29

UV-A AND UV-B FLUORESCENT LAMPS

Applicant Zip Tan

K-Number K828054

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N/A 1982-09-29

MAMMOMAT B AND BE

Applicant Siemens Medical Solutions USA, Inc.

K-Number K828055

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KNT 1982-09-28

NEEDLE CATHETER JEJUNOSTOMY KIT

Applicant Bio-Research Associates, Inc.

K-Number K822565

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DQO 1982-09-28

POLYETHYLENE CARDIOVASCULAR CATHETER

Applicant Vertex Medical Corp.

K-Number K822594

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EKP 1982-09-28

ROOT CANAL REAMERS, TYPE K

Applicant Union Broach, Div. Moyco Industries, Inc.

K-Number K822620

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DRE 1982-09-28

VESSEL DILATOR

Applicant Vertex Medical Corp.

K-Number K822595

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DSB 1982-09-28

CUTANEOUS PRESSURE PLETHYSMOGRAPH

Applicant Life Sciences Manufacturing, Inc.

K-Number K822522

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CFP 1982-09-28

COVALENT COAT RIA KIT

Applicant Immuchem Corp.

K-Number K822509

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EBG 1982-09-28

PROTEMP

Applicant Espe GmbH (Us)

K-Number K822452

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HHD 1982-09-28

U.V.A.C. CURETTES

Applicant American Hospital Supply Corp.

K-Number K822756

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