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

N/A 1979-09-20

AF/SYSTEM

Applicant Ariel

K-Number K791192

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DXY 1979-09-20

PROGRAMMER, MEDTRONIC MODEL 5984/5985

Applicant Medtronic Vascular

K-Number K791181

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DXY 1979-09-20

MODEL 221 PROGRAMALITH PULSE GENERATOR

Applicant Pacesetter Systems

K-Number K790873

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CBK 1979-09-19

VICKERS MEDICAL MODEL 130 NEAVENT-NEO

Applicant Vickers America Medical Corp.

K-Number K791713

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CAE 1979-09-19

CONPHAR AIRWAYS

Applicant Conphar, Inc.

K-Number K791799

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BXN 1979-09-19

BARD BIOMEDICAL NERVE LOCATOR

Applicant C.R. Bard, Inc.

K-Number K791442

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GEC 1979-09-19

MEROCEL INSTRUMENT WIPE

Applicant Xomed, Inc.

K-Number K791736

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GKH 1979-09-19

ROYCO MODEL 371 SUPER DILUTOR

Applicant Royco Instruments

K-Number K791644

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DXY 1979-09-19

IMPLANTABLE PULSE GENERATOR PACEMAKERS

Applicant Intermedics, Inc.

K-Number K791568

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CAW 1979-09-19

LINDE OXYGEN CONCENTRATOR LOC-II

Applicant Union Carbide Corp.

K-Number K791437

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CAP 1979-09-19

RESPIRATOR DISCONNECT ALARM VA-100

Applicant Intersect Medical Products, Inc.

K-Number K791561

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DTA 1979-09-19

VA 1000

Applicant Vitatron Medical BV

K-Number K791380

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