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

GEN 1980-03-12

HEMOSTATIC/TUBE OCCLUDING FORCEPS

Applicant Dravon Medical, Inc.

K-Number K800435

View Details →

JSK 1980-03-12

BORDETELLA SELECTIVE SUPPLEMENT

Applicant Oxoid U.S.A., Inc.

K-Number K800265

View Details →

HPX 1980-03-12

DURALITE LENS

Applicant American Optical Corp.

K-Number K800192

View Details →

JSK 1980-03-12

STREPTOCOCCUS SUPPLEMENT

Applicant Oxoid U.S.A., Inc.

K-Number K800260

View Details →

GBW 1980-03-12

ADT MINI PERITONEAL LAVAGE KIT

Applicant A.D.T. Lab Industries

K-Number K800422

View Details →

JSK 1980-03-12

STAPHYLOCOCCI/STREPTOCOCCI SUPPLEMENT

Applicant Oxoid U.S.A., Inc.

K-Number K800258

View Details →

GDY 1980-03-12

MEDSPEC PACKING GAUZE

Applicant Medspec Corp.

K-Number K800281

View Details →

EBI 1980-03-12

MAXUM DENTURE RESIN

Applicant Dentsply Intl.

K-Number K800400

View Details →

JSK 1980-03-12

STERILE GC SUPPLEMENT

Applicant Oxoid U.S.A., Inc.

K-Number K800252

View Details →

DKX 1980-03-12

ULTRASONIC DIAGNOSTIC SYSTEM, MOD. 202

Applicant Hoffrel Instruments, Inc.

K-Number K800364

View Details →

HQG 1980-03-12

THE LENS OR OMMI-GARD

Applicant Gentex Corporation

K-Number K800521

View Details →

JSK 1980-03-12

MYCOPLASMA SUPPLEMENT G

Applicant Oxoid U.S.A., Inc.

K-Number K800253

View Details →

Page 13466 of 14146

↑