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

FPA 1979-03-06

FILTERSET 0.22, I.V. PUMP

Applicant Imed Corp.

K-Number K790108

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FPB 1979-03-06

FLUID ADMINISTRATION SETS, 15 MICRON

Applicant Medex, Inc.

K-Number K790314

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JLB 1979-03-02

UNITEST CREATINE KINASE

Applicant Boehringer Mannheim Corp.

K-Number K782156

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KLT 1979-03-02

EMIT AED ASSAYS 3500 COMPUTER DIRECTED

Applicant Syva Co.

K-Number K790255

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DIF 1979-03-02

THERA CHEM

Applicant Fisher Scientific Co., LLC

K-Number K782128

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DRR 1979-03-02

INTERVAL TIMER MODEL V4295

Applicant Electronics For Medicine, Inc.

K-Number K790203

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JLS 1979-03-02

RIA KIT, PROGESTERONE

Applicant The Upjohn Co.

K-Number K782009

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CIW 1979-03-02

UNITEST AMYLASE

Applicant Boehringer Mannheim Corp.

K-Number K782032

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DXO 1979-03-02

DIGITAL BPM

Applicant Narco Air-Shields

K-Number K790036

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JQG 1979-03-02

SPINSEP-FE59

Applicant Nuclear Diagnostics, Inc.

K-Number K790133

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EBI 1979-03-02

REPRODENT

Applicant Premier Dental Products Co.

K-Number K790325

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GZJ 1979-03-02

STIMULATOR, MENTOR 100 NERVE

Applicant Mentor Corp.

K-Number K790011

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