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

CCL 1981-09-21

OXYGEN MONITOR 140/141

Applicant Medix Medical Electronics (U.S.A.), Inc.

K-Number K812040

View Details →

HMF 1981-09-21

RELIANCE OPHTHALMIC INSTRUMENT CONTROL

Applicant F. & F. Koenigkramer

K-Number K812544

View Details →

HPX 1981-09-21

LENSINE EXTRA STRENGTH CLEANER

Applicant CooperVision, Inc.

K-Number K812433

View Details →

DRT 1981-09-21

PORTAPULSE

Applicant Gavon, Inc.

K-Number K812131

View Details →

CAX 1981-09-21

PRESET FLOWMETER

Applicant Timeter Instrument Corp.

K-Number K812419

View Details →

HFC 1981-09-21

ENDOCERVICAL ASPIRATOR

Applicant Fertility Instrumentation, Inc.

K-Number K812175

View Details →

EGG 1981-09-21

PRECIOUS-METAL/PLASTIC ATTACH., AUXILL

Applicant Zl-Microdent-Attachments

K-Number K812360

View Details →

LDF 1981-09-21

USCI TRANSTHORACIC TEMP. PACING ELECTROD

Applicant C.R. Bard, Inc.

K-Number K812307

View Details →

JOH 1981-09-21

AIRE-CUF TRACHEOSTOMY TUBE

Applicant Bioana Surgical Instruments, Inc.

K-Number K812163

View Details →

FPB 1981-09-21

HIFLO-HP

Applicant Tri-Med, Inc.

K-Number K812457

View Details →

KDI 1981-09-21

C-DAK DUO-FLUX ARTIFICIAL KIDNEY

Applicant Cordis Corp.

K-Number K811830

View Details →

DXN 1981-09-21

NIVP MONITOR

Applicant Datascope Corp.

K-Number K812259

View Details →

Page 13079 of 14150

↑