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

KPP 1981-03-13

KPP PERITONEAL DIALYSATE FILTER

Applicant Millipore Corp.

K-Number K803275

View Details →

IPF 1981-03-13

VERI/PMS MODEL 815

Applicant Verite

K-Number K810496

View Details →

DXY 1981-03-13

THINLITH II PULSE GNEERATOR MODEL 227-05

Applicant Intermedics, Inc.

K-Number K810386

View Details →

BTA 1981-03-13

GOMCO SUCTION PUMP CABINET CHANGE

Applicant Allied Healthcare Products, Inc.

K-Number K810490

View Details →

GZJ 1981-03-13

NEUROPAC ULTRA I

Applicant Medical Devices, Inc.

K-Number K810593

View Details →

FJS 1981-03-13

MIROMED PERITONEAL DIALYSIS CATHETER

Applicant American Medical Products, Inc.

K-Number K810236

View Details →

IPY 1981-03-13

SPINAL EXTENSION BRACE

Applicant Orthomedics

K-Number K810556

View Details →

OLT 1981-03-13

ELECTROENCEPHALOMYOGRAPH

Applicant Thoracel Research Labs.

K-Number K810359

View Details →

HSB 1981-03-13

MOURADIAN MODIFIED ZICKEL HUMERAL ROD

Applicant Howmedica Corp.

K-Number K810535

View Details →

JPK 1981-03-13

THROMBO-TEST (X)

Applicant Medtro GmbH

K-Number K801054

View Details →

KQM 1981-03-13

MEDISEAL CAMERA COVERS

Applicant Janin Group, Inc.

K-Number K810512

View Details →

FKW 1981-03-13

VESSEL TIPS, SIZES 13-18

Applicant Quinton, Inc.

K-Number K810257

View Details →

Page 13225 of 14150

↑