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

HWC 1978-02-23

ORTHOPEDIC DEVICES

Applicant Biomet, Inc.

K-Number K780235

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JER 1978-02-23

ORABRITE

Applicant Norcliff Thayer, Inc.

K-Number K780174

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KHQ 1978-02-23

T3 STI KIT

Applicant Polysciences, Inc.

K-Number K780146

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HST 1978-02-23

TRACTION WEIGHT BAGS

Applicant Biomet, Inc.

K-Number K780233

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JJJ 1978-02-23

LIQUID SCINTILLATION COUNTER

Applicant Roche Medical Electronics, Inc.

K-Number K780179

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ILZ 1978-02-23

TRACTION BELT, PELVIC

Applicant Biomet, Inc.

K-Number K780234

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DON 1978-02-23

LIQUISOL DIGOXIN RIA TEST KIT

Applicant Damon Corp.

K-Number K780207

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JJQ 1978-02-23

SPECTROPHOTOMETER, MODEL 380

Applicant Turner Assoc.

K-Number K780156

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HOZ 1978-02-23

MICROSPEARS

Applicant Sparta Instrument Corp.

K-Number K780257

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HST 1978-02-23

TRACTION UNITS

Applicant Biomet, Inc.

K-Number K780228

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JJT 1978-02-23

ISOENZYME SERUM CONTROL

Applicant Corning Medical & Scientific

K-Number K780147

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HAM 1978-02-23

ELECTRODE, DISPERSIVE, DISP. NEOPAD

Applicant Neomed Corp.

K-Number K780118

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