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

GAB 1983-08-16

ANCHOR BRAND SURGICAL NEEDLES

Applicant Anchor Products Co.

K-Number K831648

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FRN 1983-08-16

FLO-GARD 8500 MICROINFUSION PUMP

Applicant Travenol Laboratories, S.A.

K-Number K832166

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HCC 1983-08-16

TA-400 TEMP. FEEDBACK DEVICE

Applicant Spectral Data Systems

K-Number K832146

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ITG 1983-08-16

ORTHOPEDIC CASTING TAPE MAXCAST

Applicant Cutter Laboratories, Inc.

K-Number K832237

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JFC 1983-08-16

TEXAS INTERFACE PRESSURE EVALUATOR-TIPE

Applicant Tee-Kay Applied Technology

K-Number K831800

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DNH 1983-08-16

HC40/HC75 CATION EXCHANGE RESIN

Applicant Hamilton Co.

K-Number K832199

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JFB 1983-08-16

MASSAGE TABLE AAT-100

Applicant R&D Systems, Inc.

K-Number K832464

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N/A 1983-08-16

SETS & TRAYS

Applicant I M, Inc.

K-Number K831794

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CDM 1983-08-16

FITKIT I CHECKUP KIT

Applicant Boditestor

K-Number K830340

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N/A 1983-08-16

LENSOMETER

Applicant CooperVision, Inc.

K-Number K832085

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FPB 1983-08-16

CONTINU-FLO SOLUTION ADMINISTRATION

Applicant Travenol Laboratories, S.A.

K-Number K831668

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FLL 1983-08-16

A.M.S. TEMP. SCAN 300

Applicant Andon Medical Systems, Inc.

K-Number K832135

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