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

NQQ 2020-09-02

ApolloVue S100 Image System

Applicant Apollo Medical Optics, Ltd.

K-Number K201552

View Details →

NHA 2020-09-02

LOCATOR R-Tx

Applicant Ivory Super Holdco, Incp.

K-Number K200827

View Details →

KFM 2020-09-02

Quantum PureFlow Centrifugal Blood Pump CP37, Quantum PureFlow Centrifugal Blood Pump CP22

Applicant Qura S.R.L

K-Number K202169

View Details →

NRY 2020-09-02

ZOOM (71, 55, 45, 35) Reperfusion Catheters; ZOOM Aspiration Tubing

Applicant Imperative Care, Inc.

K-Number K202182

View Details →

OBJ 2020-09-02

VeriSight Intracardiac Echocardiography (ICE) Catheter, VeriSight Pro ICE Catheter

Applicant Philips Image Guided Therapy Corporation

K-Number K200812

View Details →

FZP 2020-09-02

Aesculap PAS-Port Proximal Anastomosis System

Applicant Aesculap, Inc.

K-Number K202124

View Details →

MLO 2020-09-02

RX-1 Rhythm Express Remote Cardiac Monitoring System

Applicant VivaQuant, Inc.

K-Number K200833

View Details →

QMI 2020-09-02

cobas BKV, cobas EBV/BKV Control Kit, cobas Buffer Negative Control Kit

Applicant Roche Molecular Systems, Inc.

K-Number K202215

View Details →

EBG 2020-09-02

Bright Temporary C&B

Applicant Dmp Dental Industry S.A.

K-Number K192830

View Details →

IYN 2020-09-02

EPIQ Series Diagnostic Ultrasound Systems

Applicant Philips Ultrasound, Inc.

K-Number K202216

View Details →

OBO 2020-09-02

OCT-Camera ID 21101A3

Applicant Optomedical Technologies GmbH

K-Number K200516

View Details →

HRS 2020-09-02

Arthrex Mesh Plates

Applicant Arthrex, Inc.

K-Number K201677

View Details →

Page 1582 of 2744

↑