FDA 510(k) FDA class 1 Substantially Equivalent 🇩🇰 Denmark

CALIBRATION KIT

K Number: K911264 · Decision Aug 2, 1991
Classifications
1
FEI Numbers
60
Registration Numbers
60
Same Product Code
31
Applicant Total
46
Review Days
144

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Basic Information

Device Name
CALIBRATION KIT
K Number
K911264
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.6400
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
S & W Medico Teknik
Date Received
March 11, 1991
Decision Date
August 2, 1991
Product Code
BXK
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
BXK Gas, Calibration (Specified Concentration)

Similar 510(k) Clearances

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Other Clearances by S & W Medico Teknik

K Number Device Name
K940933 9267 SPO2 ATHENA MODULE
K913013 TCPO2 9260 MODULE - SYSTEM ATHENA
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
Search all 46 clearances from S & W Medico Teknik →