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MODIFICATION TO KION ANESTHESIA SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K001315
510(k) Type
Special
Applicant
SIEMENS ELEMA AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/2000
Days to Decision
30 days
Submission Type
Summary

MODIFICATION TO KION ANESTHESIA SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K001315
510(k) Type
Special
Applicant
SIEMENS ELEMA AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/2000
Days to Decision
30 days
Submission Type
Summary