FDA 510(k) FDA class 2 Substantially Equivalent - Subject to Tracking Reg. 🇺🇸 United States

SERVO VENTILATOR 300 COMPUTER INTERFACE

K Number: K960010 · Decision Oct 25, 1996
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
504
Applicant Total
63
Review Days
297

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
SERVO VENTILATOR 300 COMPUTER INTERFACE
K Number
K960010
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5895
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent - Subject to Tracking Reg.
Applicant
Siemens Elema AB
Date Received
January 2, 1996
Decision Date
October 25, 1996
Product Code
CBK
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CBK Ventilator, Continuous, Facility Use

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CBK), 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
K002137 CATHCOR DESKTOP
K001315 MODIFICATION TO KION ANESTHESIA SYSTEM
K970839 SERVO VENTILATOR 300A
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 →