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

DTB 1979-09-19

IMPLANTABLE ENDOCARDIAL SCREW-IN ELEC

Applicant Oscor, Inc.

K-Number K791732

View Details →

ELC 1979-09-19

MODEL G-61 ULTRASONIC DENTAL UNIT

Applicant Cavitron Corp.

K-Number K791585

View Details →

KQN 1979-09-19

ANGIOTENSIN CONVERTING ENZYME ASSAY SYS

Applicant Ventrex Laboratories, Inc.

K-Number K791712

View Details →

DTB 1979-09-19

VENTRICULAR LEAD, MODEL 6959

Applicant Medtronic Vascular

K-Number K790143

View Details →

ESD 1979-09-19

MODEL 344

Applicant Telex Communications, Inc.

K-Number K791506

View Details →

DTB 1979-09-19

MEDTRONIC MODEL 6957

Applicant Medtronic Vascular

K-Number K791769

View Details →

ESD 1979-09-19

DAHLBERG HEARING AID MODEL UN

Applicant Dahlberg Electronics, Inc.

K-Number K791311

View Details →

GAD 1979-09-19

SCOTTS SURGICAL RETRACTOR AND ELASTIC

Applicant Lone Star Medical Products, Inc.

K-Number K791665

View Details →

BSZ 1979-09-19

OHIO MODULAR ANESTHESIA GAS MACHINE

Applicant Ohio Medical Products

K-Number K791530

View Details →

EFD 1979-09-19

AMALGAMATOR MODEL SDC--

Applicant Sierra Laboratories, Inc.

K-Number K791410

View Details →

JAY 1979-09-19

TUBE-STRAP

Applicant Olympic Medical Corp.

K-Number K791781

View Details →

CAP 1979-09-19

RESPIRATOR DISCONNECT ALARM CR201

Applicant Intersect Medical Products, Inc.

K-Number K791527

View Details →

Page 13581 of 14142

↑