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

BWF 1979-10-01

MOTIVATOR

Applicant Puritan Bennett Corp.

K-Number K791842

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FMC 1979-10-01

CONPHAR EXAM. GLOVES, POLYETHYLENE

Applicant Conphar, Inc.

K-Number K791805

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HCH 1979-10-01

SCOVILLE-LEWIS ANEURYSM CLIPS

Applicant Codman & Shurtleff, Inc.

K-Number K791764

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KIA 1979-10-01

PLASTIC SHOWER GUARD

Applicant B & F Medical Products, Inc.

K-Number K791646

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BYX 1979-10-01

RED CAP, M-502

Applicant Mem Medical, Inc.

K-Number K791851

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CBP 1979-10-01

ONE-WAY VALVE-MALE, M-504

Applicant Mem Medical, Inc.

K-Number K791849

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JSH 1979-10-01

DNASE TEST AGAR W/METHYL GREEN

Applicant Isle Media and Sterile Products, Inc.

K-Number K791813

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N/A 1979-09-28

SUGITA ANEURYSM CLIPS, APPLIERS & CASE

Applicant Codman & Shurtleff, Inc.

K-Number K791978

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HSD 1979-09-28

REXTON HS(HEARING SYSTEM)

Applicant Argosy Intl. (Usa), Inc.

K-Number K791548

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DXY 1979-09-28

PULSE GENERATORS, MODELS 5983, 5989

Applicant Medtronic Vascular

K-Number K790068

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ESD 1979-09-28

MODEL 33A HEARING AIDS

Applicant Telex Communications, Inc.

K-Number K791600

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NRQ 1979-09-28

MITER ENDOSTEAL BLADE IMPLANT

Applicant Depuy, Inc.

K-Number K791204

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