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

DRT 1982-06-17

CR-9

Applicant Life Science Instrumentation, Inc.

K-Number K821223

View Details →

DXT 1982-06-17

MALLINCKRODT DIAG. MEDIA WARMER

Applicant Forma Scientific, Inc.

K-Number K821401

View Details →

DTC 1982-06-17

MEDTRONIC A-V PACING SYSTEM ANALYZER

Applicant Medtronic Vascular

K-Number K812262

View Details →

DTM 1982-06-17

PEDIATRIC ARTERIAL BLOOD FILTER #AF-540

Applicant Bentley Laboratories, Inc.

K-Number K820679

View Details →

DRX 1982-06-17

MEDICOTEST ECG ELECTRODES

Applicant Medicotest, Inc.

K-Number K821506

View Details →

DRG 1982-06-17

EXERCISE ECG ELECTRODES, REUSABLE

Applicant Respironics, Inc.

K-Number K821384

View Details →

DTN 1982-06-17

WILLIAM HARVEY FLEX. VENOUS RESERVOIR

Applicant C.R. Bard, Inc.

K-Number K821442

View Details →

DQY 1982-06-17

RIGHT ATRIAL CATHETERS PARENTERAL NUTRIT

Applicant The Healthcare Group Laboratories, Inc.

K-Number K821480

View Details →

BTR 1982-06-17

ENDOTRACHEAL TUBE

Applicant Life-Line Products, Inc.

K-Number K821456

View Details →

DTM 1982-06-17

ARTERIAL BLOOD FILTER MODEL #AF-1040

Applicant Bentley Laboratories, Inc.

K-Number K820343

View Details →

FOZ 1982-06-16

DESERET ANGIO GUIDE

Applicant Warner-Lambert Co.

K-Number K821577

View Details →

KDD 1982-06-16

STERILE TRACHEOSTOMY CARE KIT

Applicant Pro-Pak

K-Number K821501

View Details →

Page 12872 of 14150

↑