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

JDI 1982-09-14

ZIMMER METAL BACKED ACETABULAR CUP

Applicant Zimmer, Inc.

K-Number K821893

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GKG 1982-09-14

HCT CENTRIFUGE

Applicant Boehringer Mannheim Corp.

K-Number K822445

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JTQ 1982-09-14

WATER BATH

Applicant Boekel Industries, Inc.

K-Number K822564

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JSK 1982-09-14

G-N ANAEROBE SUPPLEMENT

Applicant Oxoid U.S.A., Inc.

K-Number K822462

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EBF 1982-09-14

VISIO-OPAQUER

Applicant Espe GmbH (Us)

K-Number K822453

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JWX 1982-09-14

LSM AGAR

Applicant Granite Diagnostics, Inc.

K-Number K822558

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JSK 1982-09-14

LCAT ANTIBIOTIC SUPPLEMENT

Applicant Oxoid U.S.A., Inc.

K-Number K822460

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ESD 1982-09-14

BEHIND-THE-EAR MODEL 115 V AGC O W

Applicant Danavox, Inc.

K-Number K822655

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JHI 1982-09-14

B-HCG RADIOIMMUNOASSAY KIT

Applicant Bioclinical Group

K-Number K822515

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JSK 1982-09-14

N-S ANAEROBE SUPPLEMENT

Applicant Oxoid U.S.A., Inc.

K-Number K822461

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FSE 1982-09-14

SELF-CONTAINED MOBILE OPHTHAL. OPER. .

Applicant Surgi-Quip Inc.U

K-Number K822427

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DRT 1982-09-14

RE1000 HEART RATE MONITOR

Applicant Electronic Monitors, Inc.

K-Number K822319

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