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

SERVO ANESTHESIA CIRCLE 985

K Number: K893786 · Decision Sep 22, 1989
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
504
Applicant Total
6
Review Days
123

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 ANESTHESIA CIRCLE 985
K Number
K893786
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5895
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Siemens Life Support Systems
Date Received
May 22, 1989
Decision Date
September 22, 1989
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 Life Support Systems

K Number Device Name
K902859 SERVO VENTILATOR 300
K903991 PCM ANESTHESIA
K901474 ANESTHESIA WORKSTATION
K890932 CAV 3.0C SOFTWARE PROGRAM
K890921 DATA EXCHANGE SYSTEM, MODEL 24