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

EBF 1983-03-17

MICRODAPT DENTAL RESTORATIVE

Applicant Johnson & Johnson Professionals, Inc.

K-Number K830380

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BXB 1983-03-17

SUTTER CPM 2000

Applicant Sutter Biomedical, Inc.

K-Number K830649

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KKX 1983-03-17

STERILE SURGICAL DRAPES

Applicant Phoenix Glove Co.

K-Number K830660

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DGC 1983-03-17

RADIOIMMUNOASSAY IMMUNOGLOBULINS D.E

Applicant Clinetics Corp.

K-Number K830357

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NAD 1983-03-17

CHESEBROUGH-POND'S MULTILAYER ELASTIC

Applicant Chesebrough-Pond'S U.S.A. Co.

K-Number K823852

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FOZ 1983-03-17

INTRAVASCULAR CATHETER SET

Applicant Lab-A-Cath Corp.

K-Number K830539

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FRG 1983-03-17

RENNCO MODEL LS LIFT SEAL HEAT SEALER

Applicant Rennco, Inc.

K-Number K830540

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LIL 1983-03-17

BEDSIDE N.P.T. 9900 - PRINTER 9800

Applicant Browne Medical, Inc.

K-Number K830221

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JCA 1983-03-17

BLEEDING TIME DEVICE DISPOSABLE

Applicant American Dade

K-Number K830645

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DQO 1983-03-17

LYMPHANGIOGRAPHY SET

Applicant Vertex Medical Corp.

K-Number K830576

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N/A 1983-03-17

ARMEX LS-51

Applicant Elscint, Inc.

K-Number K837175

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ETD 1983-03-17

T-TUBE VENT TUBE

Applicant Treace Medical, Inc.

K-Number K823909

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