FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CATHCOR DESKTOP

K Number: K002137 · Decision Oct 5, 2000
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
403
Applicant Total
63
Review Days
83

Basic Information

Device Name
CATHCOR DESKTOP
K Number
K002137
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1425
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SIEMENS ELEMA AB
Date Received
July 14, 2000
Decision Date
October 5, 2000
Product Code
DQK
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
DQK Computer, Diagnostic, Programmable

Similar 510(k) Clearances

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

View all

Other Clearances by SIEMENS ELEMA AB

K Number Device Name
K023354 COMPRESSOR MINI, 115 V, MODEL 64 81 779 EH81E
K010923 KION ANAESTHESIA SYSTEM, MODEL 65 03 879 E392E
K010925 SERVOI VENTILATOR SYSTEM, MODEL 64 87 800 E407E
K001315 MODIFICATION TO KION ANESTHESIA SYSTEM
K970839 SERVO VENTILATOR 300A
K960010 SERVO VENTILATOR 300 COMPUTER INTERFACE
K960168 SIEMENS SERVO SCREEN 390 AND SERVO COMPUTER MODULE 990
K872278 SIEMENS O2-AIR MIXER 965
K871354 SERVO VENTILATOR 900 C/D
K871829 SIEMENS DRY AIR COMPRESSOR
Search all 63 clearances from SIEMENS ELEMA AB →