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ORTHOPANTOMOGRAPH OP200, OP200D, AND ORTHOCEPH OC200, OC200D

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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