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

CFH 1979-01-26

HYCEL LDH-INT TEST

Applicant Hycel, Inc.

K-Number K782176

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ESD 1979-01-26

MODULE PERSONAL EAR (COMPRESSION)

Applicant Qualitone

K-Number K790094

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JTO 1979-01-26

DISK, BETA-LACTAM

Applicant Remel Co.

K-Number K790038

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JXG 1979-01-26

VALVE, H-H CRUCIFORM SLIT

Applicant Holter-Hausner Intl.

K-Number K790126

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DHR 1979-01-26

RHEUMOGEN TEST SYSTEM

Applicant Calbiochem-Behring Corp.

K-Number K790012

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CAZ 1979-01-26

POSITIVE PLACEMENT ANETHESIA KIT

Applicant Arrow Intl., Inc.

K-Number K781469

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HQC 1979-01-26

LEVIGATOR, KEELER PHOKO

Applicant Keeler Optical Products , Ltd.

K-Number K782141

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HKN 1979-01-26

FUL-VUE

Applicant American Optical Corp.

K-Number K782118

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HPL 1979-01-26

VISION-STIMULATOR, CAM

Applicant Clement Clarke, Inc.

K-Number K781313

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HLM 1979-01-26

INSTRUMENTS, OVERREFRACTION SYSTEM

Applicant Zeiss Humphrey System

K-Number K782096

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IYO 1979-01-25

SCANNER-SV

Applicant Hrl, Inc.

K-Number K782158

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DQO 1979-01-25

ARTERIAL EXTENSION SET

Applicant Namic

K-Number K790082

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