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

EPY 1982-08-11

EAR SPECULI

Applicant Kelleher Corp.

K-Number K822164

View Details →

BTR 1982-08-10

SHERIDAN/HVT,CF, UNCUFFED

Applicant Sheridan Catheter Corp.

K-Number K822082

View Details →

HLI 1982-08-10

ALCON INDIRECT OPHTHALMOSCOPE

Applicant Alcon Laboratories

K-Number K822104

View Details →

N/A 1982-08-10

DIGITAL FLUOROGRAPHIC X-RAY SYSTEM

Applicant General Electric Co.

K-Number K827760

View Details →

LJE 1982-08-10

SURGITEK PERCUTANEOUS NEPHROST. STENT

Applicant Medical Engineering Corp.

K-Number K821776

View Details →

FBN 1982-08-10

PENTAX CHOLEDOCHOFIBERSCOPE, #FCD-15A

Applicant Pentax Precision Instrument Corp.

K-Number K821974

View Details →

CAW 1982-08-10

SYSTEM ONE OXYGEN CONCENTRATOR

Applicant Marathon

K-Number K821393

View Details →

FAE 1982-08-10

THE INFLATABLE PENILE PROSTHESIS

Applicant American Medical Systems, Inc.

K-Number K821628

View Details →

N/A 1982-08-10

RADIOGRAPHIC FILM ILLUMINATOR

Applicant Brandt Industries, Inc.

K-Number K827762

View Details →

FGE 1982-08-10

PIGTAIL NASAL CATHETERS

Applicant American Endoscopy, Inc.

K-Number K821817

View Details →

HNN 1982-08-10

OPHTHALMIC KNIFE

Applicant Sharpoint, Inc.

K-Number K822112

View Details →

FAG 1982-08-10

THE ARTIFICIAL URINARY SPHINCTER

Applicant American Medical Systems, Inc.

K-Number K821627

View Details →

Page 12833 of 14156

↑