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

LHD 1981-06-24

FORECASTER

Applicant Forecaster Co.

K-Number K810832

View Details →

IZF 1981-06-23

SOMATOM 2N

Applicant Siemens Corp.

K-Number K811302

View Details →

FKQ 1981-06-23

MODEL DM-333 DIALYSIS CONTROL STATION

Applicant Extracorporeal Medical Specialities, Inc.

K-Number K811444

View Details →

KOC 1981-06-23

MODEL RS-8100

Applicant Rinal Systems, Inc.

K-Number K811457

View Details →

HHT 1981-06-23

CERVICAL SPATULA

Applicant Procedure Products, Inc.

K-Number K811548

View Details →

FGB 1981-06-23

MODEL FUS-1, FLEXIBLE URETEROSCOPE

Applicant American Optical Corp.

K-Number K811535

View Details →

KPR 1981-06-23

X-CELL X-RAY #'S P-75W/P-75M

Applicant X-Cel X-Ray Corp.

K-Number K811230

View Details →

JAA 1981-06-23

DIGITAL NOISE REDUCER

Applicant Philips Medical Systems (Cleveland), Inc.

K-Number K811295

View Details →

KNT 1981-06-23

AUTOMATED GASTRIC LAVAGE

Applicant Emergency Medicine

K-Number K811061

View Details →

HRS 1981-06-23

CRYOPHTHALMIC UNIT

Applicant Keeler Instruments, Inc.

K-Number K811244

View Details →

ITX 1981-06-19

7.5 MHZ WP TRANSDUCER

Applicant General Electric Co.

K-Number K810748

View Details →

FMF 1981-06-18

MONOJECT STERILE M503 3CC SYRINGES

Applicant Sherwood Medical Co.

K-Number K811505

View Details →

Page 13149 of 14150

↑