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 1982-08-24

SONOLINE 6000

Applicant Siemens Medical Solutions USA, Inc.

K-Number K827815

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N/A 1982-08-24

PODIATRY X-RAY UNIT

Applicant The S. S. White Co.

K-Number K827816

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DRT 1982-08-24

HARVEY-BOSTWICK BRADY CARDIA MONIT. HB85

Applicant Harvey-Bostwick, Inc.

K-Number K821942

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DWF 1982-08-24

SARNS CARDIOPLEGIA CANNULAE (VAR. TYPES

Applicant 3M Health Care, Sarns

K-Number K822210

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FTC 1982-08-23

FOLDALITE UNIT

Applicant National Biological Corp.

K-Number K827890

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FFZ 1982-08-20

ELECTRIC CORD FOR ENDOSCOPE

Applicant Kelleher Corp.

K-Number K822254

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N/A 1982-08-20

DOPPLER FLOW METER, LASER

Applicant Atl Interspec Cardiology

K-Number K827818

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HTH 1982-08-20

ORTHO-LEVEL

Applicant Frontier Products

K-Number K822305

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BTO 1982-08-20

SURGI TEK'S DISPOS. INNER CANNULA FOR

Applicant Medical Engineering Corp.

K-Number K822295

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FGE 1982-08-20

PIGTAIL STENTS

Applicant American Endoscopy, Inc.

K-Number K821819

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HBM 1982-08-20

SURGICAL HEAD SUPPORT

Applicant Kelleher Corp.

K-Number K822169

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JDI 1982-08-20

POROCOAT LOW PROFILE METAL BACKED CUP

Applicant Depuy, Inc.

K-Number K821713

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