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DINAMAP PRO 1000 MONITOR, MODEL 1000

Page Type
Cleared 510(K)
510(k) Number
K002248
510(k) Type
Traditional
Applicant
CRITIKON COMPANY,LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2000
Days to Decision
58 days
Submission Type
Summary

DINAMAP PRO 1000 MONITOR, MODEL 1000

Page Type
Cleared 510(K)
510(k) Number
K002248
510(k) Type
Traditional
Applicant
CRITIKON COMPANY,LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2000
Days to Decision
58 days
Submission Type
Summary