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

CDO 1979-01-03

ACID REAGENT, URIC SINGLE VIAL

Applicant Calbiochem-Behring Corp.

K-Number K781996

View Details →

CHL 1979-01-03

BLOOD GAS SYSTEM MODEL 168

Applicant Corning Medical & Scientific

K-Number K781968

View Details →

HDY 1979-01-03

DILATOR, MIZUTANI LAMINARIA TENT

Applicant British Marketing Ent., Ltd.

K-Number K782067

View Details →

KHQ 1979-01-03

RIA KIT, QUANTITOPE T3 UPTAKE

Applicant Kallestad Laboratories, Inc.

K-Number K781905

View Details →

DNL 1979-01-03

TEST SET, 125 I-DIGOXIN

Applicant Wien Laboratories, Inc.

K-Number K781834

View Details →

DOZ 1979-01-03

ANALYSIS SYSTEM, PREP SAMPLE

Applicant E.I. Dupont DE Nemours & Co., Inc.

K-Number K781941

View Details →

CGI 1979-01-03

RIA, QUANTIMUNE E3

Applicant Bio-Rad

K-Number K781850

View Details →

LAS 1979-01-03

CONTROL SET, EMIT METHOTREXATE

Applicant Syva Co.

K-Number K781827

View Details →

IYO 1979-01-03

ULTRASOUND BREAST SCANNING DEVICE

Applicant Life Instrument Corp.

K-Number K781177

View Details →

FZE 1979-01-03

PASTE, PRO CARE PROPHYLAXIS

Applicant Young Dental Manufacturing Co. 1, LLC

K-Number K782104

View Details →

GKZ 1979-01-03

PRINTER, TEK PRO TEK TALLY II

Applicant Tekpro

K-Number K782050

View Details →

JPK 1979-01-03

BLOOD, HEMATOLOGY REFERENCE CONTROL

Applicant Coulter Electronics, Inc.

K-Number K781969

View Details →

Page 13710 of 14142

↑