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

DYB 1981-11-16

INTRODUCER, PERCUTANEOUS SELDINGER

Applicant Triad Medical Division

K-Number K812964

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DYG 1981-11-16

PRUITT ARTERIAL OCCLUSION CHOLANG. CATH

Applicant Bionomy, Inc.

K-Number K812111

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GDJ 1981-11-16

SURGICAL PAWS

Applicant Berkeley Medevices

K-Number K812388

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GGP 1981-11-16

LANCER COAGENT HUMAN VACTOR VIII PLASMA

Applicant Sherwood Medical Co.

K-Number K812975

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MDM 1981-11-16

SILICONE IMPLANTS

Applicant Sutter Biomedical, Inc.

K-Number K812691

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JPA 1981-11-16

DIGICLOT 2-#820

Applicant Volu Sol Medical Industries

K-Number K812121

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HQF 1981-11-16

MODEL 900S INTRAOCULAR PROBE

Applicant Lumenis, Inc.

K-Number K812219

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ITX 1981-11-16

VARIABLE FOCUS 3.5 MHZ TRANSDUCER

Applicant Adr Ultrasound

K-Number K812301

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BXW 1981-11-16

DATASCRIBE #DS-40

Applicant Timeter Instrument Corp.

K-Number K812765

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DQO 1981-11-16

PET POLYETHYLENE TORQUE CATHETER

Applicant Universal Medical Instrument Corp.

K-Number K812999

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LDF 1981-11-16

MODEL 5867-12 BIPOLAR LOW-PROFILE LEAD

Applicant Medtronic Vascular

K-Number K812725

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DYB 1981-11-16

PERCUTANEOUS INTRODUCER COURNAND STYLE

Applicant Dip, Inc.

K-Number K812973

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