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

JDI 1980-12-16

ORTRON 90* HIP PROSTHESIS

Applicant Cintor Orthopaedic Div.

K-Number K802627

View Details →

EWG 1980-12-15

VIDA 55 PULSE-ECHO ULTRASONIC DEVICE

Applicant Vida, Inc.

K-Number K802279

View Details →

FIP 1980-12-15

CMR 300, ROWATER TREATMENT UNIT

Applicant U-Marc, Inc.

K-Number K802474

View Details →

HST 1980-12-12

UPPER EXTREMITY TRACTION DEVICE

Applicant Orthopedic Systems, Inc.

K-Number K803021

View Details →

JSK 1980-12-11

CAMPYLOBACTER SELECTIVE SUPPLEMENT (BL.)

Applicant Oxoid U.S.A., Inc.

K-Number K802753

View Details →

JDI 1980-12-11

AUFRANC-TURNER ATS TOTAL HIP SYSTEM

Applicant Howmedica Corp.

K-Number K802872

View Details →

EFQ 1980-12-11

GAUZE PADS STERILE SINGLES

Applicant Abco Dealers, Inc.

K-Number K802862

View Details →

IYO 1980-12-11

SIAM 80-INSTANTANEOUS SONOGRAPH W/STOR.

Applicant Cgr Medical Corp.

K-Number K802704

View Details →

GKL 1980-12-11

PLATELET COUNTING KIT

Applicant Streck Laboratories, Inc.

K-Number K802636

View Details →

DTR 1980-12-11

CARDIOPLEGIA COOLING SYST. CCAS-2

Applicant Bentley Laboratories, Inc.

K-Number K802848

View Details →

CDZ 1980-12-11

125I-TESTOSTERONE TEST SET

Applicant Wien Laboratories, Inc.

K-Number K802728

View Details →

JIX 1980-12-11

ALBUMIN/TOTAL PROTEIN STANDARDS

Applicant Gilford Diagnostics

K-Number K802632

View Details →

Page 13294 of 14146

↑