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ORTHOPANTOMOGRAPH OP200, OP200D, AND ORTHOCEPH OC200, OC200D

Page Type
Cleared 510(K)
510(k) Number
K043612
510(k) Type
Traditional
Applicant
INSTRUMENTARIUM CORP. IMAGING DIVISION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/2005
Days to Decision
41 days
Submission Type
Summary

ORTHOPANTOMOGRAPH OP200, OP200D, AND ORTHOCEPH OC200, OC200D

Page Type
Cleared 510(K)
510(k) Number
K043612
510(k) Type
Traditional
Applicant
INSTRUMENTARIUM CORP. IMAGING DIVISION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/2005
Days to Decision
41 days
Submission Type
Summary