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

KWL 1982-08-19

KAMPNER FEMORAL COMPONENT

Applicant Intermedics Orthopedics

K-Number K822320

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HIB 1982-08-19

PRO-SPEC

Applicant Exitec, Inc.

K-Number K822084

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HNF 1982-08-19

SURGICAL INSTRUMENTS REPRESENT. 4 CLASS

Applicant Robert I. Chien & Assoc., Inc.

K-Number K822151

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GEI 1982-08-19

BALL TIP COAGULATING ELECTRODES

Applicant American Endoscopy, Inc.

K-Number K822062

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FRO 1982-08-19

SELOPOR

Applicant Selomas, Inc.

K-Number K821258

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DSP 1982-08-19

DATASCOPE 10.5 FRENCH INTRA-AORTIC BAL

Applicant Datascope Corp.

K-Number K821065

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ESD 1982-08-19

BEHIND-THE-EAR MODEL SERIES 123

Applicant Danavox, Inc.

K-Number K822387

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N/A 1982-08-16

SONOLINE 1000, 8008 AND 8080

Applicant Siemens Medical Solutions USA, Inc.

K-Number K827503

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CBK 1982-08-16

SECHRIST MODEL 990 JET VENTILATOR

Applicant Sechrist Industries, Inc.

K-Number K821930

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EPF 1982-08-16

POWERED MUSCLE STIMULATOR

Applicant High Country Ent.

K-Number K821511

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EOQ 1982-08-16

LASER BRONCHOSCOPE

Applicant Laser Industries of Tel Aviv

K-Number K822136

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KBL 1982-08-16

ENT METAL TONGUE DEPRESSORS

Applicant Kelleher Corp.

K-Number K822184

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