FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

VITALITH S 3000 SERIES

K Number: K790666 · Decision Jun 1, 1979
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
460
Applicant Total
19
Review Days
56

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
VITALITH S 3000 SERIES
K Number
K790666
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.3610
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Vitatron Medical BV
Date Received
April 6, 1979
Decision Date
June 1, 1979
Product Code
DXY
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DXY Implantable Pacemaker Pulse-Generator

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DXY), ordered by most recent decision date.

View all

Other Clearances by Vitatron Medical BV

K Number Device Name
K854790 CERYX PACEMAKER MODELS 114, 314 & 614
K844484 HEWLETT PACKARDT HP 85 W/ VITATRON PH1 PROGRAM HEA
K844483 TP 1
K844485 CERYX6, 611, CERYX 3 311 & CERYX 1 111
K840668 ELECTRODE PACEMAKER, PERM & TEMP
K831859 PACEMAKER PROGRAMMER #2032
K831860 GENERATOR, PULSE, PACEMAKER #532
K810928 ENDOCARDIAL ELECTRODE
K791920 CARDIAC PACEMAKER P4000 SER. & P1000
K791921 CARDIAC PACEMAKER C4000, C1000 SER.
Search all 19 clearances from Vitatron Medical BV →