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PROMAX, PANORAMIC X-RAY UNIT WITH CEPHALOSTAT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011619
510(k) Type
Traditional
Applicant
Planmeca Oy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/29/2001
Days to Decision
35 days
Submission Type
Statement

PROMAX, PANORAMIC X-RAY UNIT WITH CEPHALOSTAT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011619
510(k) Type
Traditional
Applicant
Planmeca Oy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/29/2001
Days to Decision
35 days
Submission Type
Statement