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

IPF 1982-09-22

MYO-TONE, INC. SYSTEM-80

Applicant Myo-Tone, Inc.

K-Number K822250

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GEI 1982-09-22

DISP. METAL & PLASTIC ELECTROSURG. DEV

Applicant Valleylab, Inc.

K-Number K822355

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FPA 1982-09-22

DISPOSABLE PLASTIC TRANSFUS./INFUS. ASSB

Applicant Valleylab, Inc.

K-Number K822354

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FLL 1982-09-22

MEDI-THERM SKIN THERMOMETER

Applicant Everest Interscience, Inc.

K-Number K822435

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DHN 1982-09-21

ANA HEP-2 FLUORO-KIT

Applicant Clinical Sciences, Inc.

K-Number K822397

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DRT 1982-09-21

LIFE WATCH LSI

Applicant Life Science Instrumentation, Inc.

K-Number K822615

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JSJ 1982-09-21

PSEUDOMONAS AGAR BASE, C-N & C-F-C SUPP

Applicant Oxoid U.S.A., Inc.

K-Number K822664

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JSJ 1982-09-21

VOGEL JOHNSON AGAR

Applicant Oxoid U.S.A., Inc.

K-Number K822660

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GDW 1982-09-21

DISPOSABLE LINEAR STAPLER (LSF)

Applicant ETHICON, Inc.

K-Number K822345

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DQX 1982-09-21

GUIDE WIRE

Applicant Vertex Medical Corp.

K-Number K822597

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DQO 1982-09-21

VERTEX PERCUTANEOUS PUNCTURE NEEDLE

Applicant Vertex Medical Corp.

K-Number K822596

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DRI 1982-09-21

HEART MONITOR BRACELET ALARM

Applicant Hmba

K-Number K822316

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