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

CBT 1983-05-25

ASPIRATOR

Applicant Marquest Medical Products, Inc.

K-Number K830312

View Details →

DTZ 1983-05-25

HI FLEX D-700 MODULAR BUBBLE OXYGENA-

Applicant Electromedics, Inc.

K-Number K830639

View Details →

DXY 1983-05-25

NEDS-01 & EPR-500

Applicant Biotronik Sales, Inc.

K-Number K830862

View Details →

IRO 1983-05-25

NORELCO VIBRATING BOARD V900

Applicant North American Philips Corp.

K-Number K830715

View Details →

DOY 1983-05-25

WALRUS PERCUTANEOUS INTRODUCER SET

Applicant Medical Parameters, Inc.

K-Number K831239

View Details →

JDI 1983-05-25

CFE TOTAL HIP FEMORAL COMPONENT

Applicant Biomet, Inc.

K-Number K830313

View Details →

FLL 1983-05-18

DISPOS. TYPE T THERMOCOUPLE TEMP.PROBE

Applicant Electromedics, Inc.

K-Number K830592

View Details →

DXH 1983-05-18

LIFE LINE

Applicant Kb & Assoc.

K-Number K830254

View Details →

JSE 1983-05-18

API 20GP

Applicant Analytical Products, Inc.

K-Number K830525

View Details →

DXN 1983-05-18

NORELCO ELECTRONIC ANALOG BLOOD PRESS

Applicant North American Philips Corp.

K-Number K830687

View Details →

KOA 1983-05-18

DISIMETRIC RELEASE OF INSTRANETICS RAD

Applicant American Convertors Div., American Pharmaseal

K-Number K830786

View Details →

N/A 1983-05-18

SHARPLAN 721 CO2 SURGICAL LASER

Applicant Laser Industries , Ltd.

K-Number K837342

View Details →

Page 12615 of 14156

↑