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

DRX 1978-09-26

ELECTRODE, DEIP.

Applicant Datascope Corp.

K-Number K781163

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IPF 1978-09-26

MUSCLE STIMULATOR, ELECTRONIC

Applicant Thor Medical Instruments, Inc.

K-Number K781139

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KOC 1978-09-26

DLC 500, DOUBLE LUMEN CATHETER

Applicant Hemodialysis, Division of The

K-Number K781050

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HGM 1978-09-26

MODEL 80032A, OBSTETRICAL TELEMETRY

Applicant Hewlett-Packard Co.

K-Number K781359

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CAX 1978-09-26

FLOMETER

Applicant Chemetron Medical Products, Inc.

K-Number K781541

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JAY 1978-09-26

ZEE-FRAME

Applicant Equilibrated Bio Systems, Inc.

K-Number K781509

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IYO 1978-09-26

WATERPATH SCANNING OPTION

Applicant G.D. Searle and Co.

K-Number K781508

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DRT 1978-09-20

CARDIOPNEUMOGRAPH

Applicant Street Electronics Corp.

K-Number K781292

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N/A 1978-09-20

STIMULATOR, NERVE, TRANSCUTANEOUS

Applicant Medtech Intl., Inc.

K-Number K781157

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BWF 1978-09-20

LUNG EXER. BAG, POST-OP, MODIFIED

Applicant Dytek Corp.

K-Number K781245

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CHW 1978-09-20

LINDE OXYGEN CONCENTRATOR MODEL LOC-HCA

Applicant Union Carbide Corp.

K-Number K781454

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DXJ 1978-09-20

CATHODE RAY TUBE MED. DISPLAY

Applicant Rae Medical Corp.

K-Number K781256

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