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

JIH 1980-01-21

LITHIUM DILUENT (1500 MM/E)

Applicant Gilford Diagnostics

K-Number K800039

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CGI 1980-01-21

TOTAL ESTRIOL RIA KIT

Applicant Amersham Corp.

K-Number K800036

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HRY 1980-01-21

LIVERPOOL KNEE PROSTHESIS

Applicant Downs Surgical , Ltd.

K-Number K792325

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IYO 1980-01-21

SMV 120 SONIC MAMMOGRAPHIC VIEWER

Applicant Johnson & Johnson Professionals, Inc.

K-Number K792585

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IGG 1980-01-21

PARA-PAK SAF

Applicant Meridian Diagnostics, Inc.

K-Number K792707

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JJX 1980-01-21

PENTEX LIPOPROTEIN CHOLESTEROL SOLU.

Applicant Miles Laboratories, Inc.

K-Number K800035

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IGG 1980-01-21

PARA-PAK FORMALIN

Applicant Meridian Diagnostics, Inc.

K-Number K792705

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BXB 1980-01-21

WORK SIMULATOR

Applicant Baltimore Therapeutic Equipment Co.

K-Number K800007

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JIS 1980-01-21

LITHIUM STANDARD (1MM/L)

Applicant Gilford Diagnostics

K-Number K800042

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KFH 1980-01-17

BLASTOMYCES DERMATITIDIS POS/CONTROL

Applicant Meridian Diagnostics, Inc.

K-Number K792681

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JKA 1980-01-17

VENOJECT AUTOSEP

Applicant Kimble-Terumo, Inc.

K-Number K792587

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JSM 1980-01-17

PARA-PAK (C&S)

Applicant Meridian Diagnostics, Inc.

K-Number K792712

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