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

HAW 2017-09-14

Fiagon Navigation System

Applicant Fiagon GmbH

K-Number K163209

View Details →

OLO 2017-09-14

VIPER PRIME navigated inserter

Applicant Medos International SARL

K-Number K170937

View Details →

KGC 2017-09-14

Entuit Start Initial Placement Gastrostomy Set

Applicant Cook Incorporated

K-Number K170323

View Details →

FHO 2017-09-14

Veress Needle

Applicant Wickimed (Huizhou) Medical Equipment Manufacturing Co.,Ltd

K-Number K172120

View Details →

JCX 2017-09-14

IntelliCart System

Applicant Dornoch Medical Systems

K-Number K172481

View Details →

HSB 2017-09-14

Shotel Ankle Arthrodesis Nail System

Applicant Biopro, Inc.

K-Number K163627

View Details →

FZP 2017-09-14

Amsel Occluder Device

Applicant Amsel Medical

K-Number K172479

View Details →

BZE 2017-09-14

AirLife Adult Heated Wire BiPAP/NIV Circuit

Applicant Vyaire Medical

K-Number K170378

View Details →

LLZ 2017-09-14

3D Echo

Applicant Jointvue, LLC

K-Number K172513

View Details →

KNW 2017-09-14

Bard Mission Disposable Core Biopsy Instrument

Applicant Bard Peripheral Vascular, Inc.

K-Number K171953

View Details →

LZA 2017-09-14

Non-Sterile, Single use, Powder-free examination glove tested for use with Chemotherapy drugs

Applicant Semperit Investments Asia Pte , Ltd.

K-Number K171378

View Details →

IYO 2017-09-13

FibroScan 430 Mini+

Applicant Echosens

K-Number K172142

View Details →

Page 2312 of 2738

↑