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

JOY 1978-01-05

RE-CELL SLIDE RECAP

Applicant Geometric Data, Div. Smithkline Corp.

K-Number K772139

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CDX 1978-01-05

RIA FOR SERUM THYROXINE

Applicant Clinical Immuno-Diagnostics

K-Number K771415

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DCB 1978-01-05

FLUORESCEIN CONJUG. FRACT. MONO. ANTI.

Applicant Kallestad Laboratories, Inc.

K-Number K772345

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ILH 1978-01-05

PRE-FORMED SPLINT BLANKS

Applicant Fred Sammons, Inc.

K-Number K772416

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DDR 1978-01-05

HEMAGGLUTINATION INHIBITION TEST

Applicant Miles Laboratories, Inc.

K-Number K772095

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CGS 1978-01-05

CLINICARD CK-II

Applicant Harleco

K-Number K772258

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ILH 1978-01-05

PLATFORM SPLINTS

Applicant Fred Sammons, Inc.

K-Number K772411

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CAN 1978-01-05

PORT-A-BOUT 240

Applicant Hudson Oxygen Therapy Sales Co.

K-Number K772216

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HRW 1978-01-05

PINCH GUAGE

Applicant Fred Sammons, Inc.

K-Number K772413

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DSK 1978-01-05

CARDIAC OUTPUT MODULE-78231C

Applicant Hewlett-Packard Co.

K-Number K772234

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HRW 1978-01-05

DYNAMETER 50 LB.

Applicant Fred Sammons, Inc.

K-Number K772415

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FPA 1978-01-05

SCALP VEIN SET

Applicant Berman, Pcp & Consultants, Inc.

K-Number K771983

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