IYY — Synchronizer, Electrocardiograph, Nuclear Class I

FDA Device Classification

FDA product code IYY covers "Synchronizer, Electrocardiograph, Nuclear", a Class I medical device regulated under 21 CFR 892.1410. Submissions are reviewed by the Radiology panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
IYY
Device Class
Class I
Regulation Number
892.1410
Submission Type
Review Panel
RA
Medical Specialty
Radiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K853737capintecVEST(AMBULATORY VENTRICULAR EVALUATING SYSTEM)February 13, 1986
K790213amrGENERATOR, R-WAVEMarch 22, 1979
K780510biosNUCLEAR STETHOSCOPEApril 18, 1978