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

DXN 1979-03-02

MODEL 1051, MONITOR

Applicant Applied Medical Research

K-Number K790328

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KLS 1979-03-02

EMIT THEOPHYLLINE ASSAY

Applicant Syva Co.

K-Number K790256

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GEI 1979-03-02

GRAB-IT

Applicant Concept, Inc.

K-Number K790367

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DWF 1979-03-02

SARNS WIRE-REINFORCED VENOUS RETURN CAN

Applicant 3M Health Care, Sarns

K-Number K790246

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BSJ 1979-03-01

THE BLUE MASK

Applicant Collectovac, Inc.

K-Number K782163

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CDD 1979-02-28

RIA KIT, VITAMIN B12

Applicant Technia Diagnostics , Ltd.

K-Number K782024

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DRT 1979-02-28

MONITOR SCOPES, MODELS 9502, 9503

Applicant C-V Monitors Corp.

K-Number K790004

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DSI 1979-02-28

ANALYZER, MEDILOG II

Applicant Oxford Medilog, Inc.

K-Number K790287

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FJS 1979-02-27

CATHETER, RADIOPAQUE TENCKHOFF

Applicant Dravon Medical, Inc.

K-Number K782057

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FNL 1979-02-27

BED, PARAPLEGIC

Applicant Wayne V. Kirkman

K-Number K790049

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ESD 1979-02-27

HEARING AID MODEL 8143

Applicant Int'L Hearing Aids, Inc.

K-Number K790270

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BZQ 1979-02-27

PREAMPLIFIER MODULE, EKG RESPIRATION

Applicant Abbott Medical Electronics Co.

K-Number K790304

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