FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇰 Denmark

TCPO2 9260 MODULE - SYSTEM ATHENA

K Number: K913013 · Decision May 3, 1994
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
16
Applicant Total
46
Review Days
1030

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Basic Information

Device Name
TCPO2 9260 MODULE - SYSTEM ATHENA
K Number
K913013
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2480
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
S & W Medico Teknik
Date Received
July 8, 1991
Decision Date
May 3, 1994
Product Code
LKD
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
LKD Monitor, Carbon-Dioxide, Cutaneous

Similar 510(k) Clearances

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

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Other Clearances by S & W Medico Teknik

K Number Device Name
K940933 9267 SPO2 ATHENA MODULE
K915633 MOD. TYPE 9230 TEMP 1 AND TEMP 2 SYSTEM ATHENA
K930134 9055 IRCA OPTION FOR SYSTEM ATHENA 9050 NT
K923418 9293/1 INTERFACE MODULE
K911611 SYSTEM ATHENA, MODIFICATION
K922314 VENTILATOR INTERFACE 9291/4
K912815 NIBP 9225 COMBI
K912000 TYPE INTERFACE 9271/1 INCUBATOR/WARMER
K912183 TYPE 9050/NEO
K912145 SYSTEM ATHENA-PRODUCT ENHANCEMENTS, ANESTHESIA
Search all 46 clearances from S & W Medico Teknik →