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

CAW 1979-12-05

DEVO OXYGEN CONCENTRATOR, MODEL 955

Applicant The Devilbiss Co.

K-Number K792385

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DTB 1979-12-05

CARDIAC PACING ELECTRODE

Applicant Medi-Dyne Instruments, Inc.

K-Number K792379

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DTL 1979-12-05

CONPHAR MANOMETER CONNECTORS

Applicant Conphar, Inc.

K-Number K792113

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HWN 1979-12-05

ARICULATED TENSION DEVICE SYNTHES TEN

Applicant Synthes (Usa)

K-Number K792253

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DXQ 1979-12-05

ANEROID SPHYMOMANOMETER

Applicant Abco Dealers, Inc.

K-Number K792355

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BYH 1979-12-04

MOISTURE TRAP

Applicant Dhd Medical Products Div. Diemolding Corp.

K-Number K792390

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GGP 1979-12-04

HELENA FACTOR VIII DEFICIENT SUB. PLASMA

Applicant Helena Laboratories

K-Number K792335

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DWP 1979-12-04

BONCHEK-SHILEY VEIN DISTENTION SYSTEM

Applicant Shiley, Inc.

K-Number K792134

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JTQ 1979-12-04

TEMPTRONIC 100 WATER BATH

Applicant Sybron Corp.

K-Number K792060

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CCL 1979-12-04

OXEQUIP MODEL 34 MED*STAR OXYGEN MONITOR

Applicant Oxequip Health Ind.

K-Number K792356

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JFH 1979-12-04

PROSTATIC ACID RADIOIMMUNOASSAY TEST

Applicant Clinical Assays, Inc.

K-Number K791497

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KSY 1979-12-04

RH VIEWBOX

Applicant Tekpro

K-Number K792306

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