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

KOC 1983-03-17

ASAHI HOLLOW FIBER KIDNEYS, AM-SERIES

Applicant Advocacy International, Ltd.

K-Number K830231

View Details →

LFX 1983-03-17

ORTHO RUBELLA ELISA TEST SYSTEM

Applicant Ortho Diagnostic Systems, Inc.

K-Number K822342

View Details →

DTB 1983-03-16

PACEMAKER ELECTRODE PERM. & TEMP

Applicant Daig Corp.

K-Number K830464

View Details →

DQO 1983-03-16

CATHETER CONNECTION W/INTEGRAL INJECTATE

Applicant Gould, Inc.

K-Number K830523

View Details →

DXY 1983-03-16

MEDTRONIC MODELS 59401 5941

Applicant Medtronic Vascular

K-Number K823831

View Details →

FED 1983-03-15

SPLIT COLON STIFFENING TUBE

Applicant Keymed, Inc.

K-Number K830247

View Details →

N/A 1983-03-14

MODEL 2100 FETAL MONITOR

Applicant Huntleigh Group , Ltd.

K-Number K837102

View Details →

N/A 1983-03-11

MODEL 4100 MICROSURGICAL CO2 LASER SYSTEM

Applicant Bio Quantum Technologies, Inc.

K-Number K837110

View Details →

KRI 1983-03-11

HOLDER FOR BOS-2S INFANT BUBBLE OXYGENA-

Applicant American Bentley

K-Number K830167

View Details →

BZW 1983-03-11

ESOPHAGEAL STETHOSCOPE

Applicant Science Development Corp.

K-Number K830329

View Details →

BYE 1983-03-11

PEEPER

Applicant Dupaco, Inc.

K-Number K830395

View Details →

DIF 1983-03-11

CONTOX DRUG SCREEN CONTROL

Applicant Kaulson Laboratories, Inc.

K-Number K830494

View Details →

Page 12671 of 14156

↑