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PM2002 CC AND PM2002 EC

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K904948
510(k) Type
Traditional
Applicant
PLANMECA USA, INC.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
1/30/1991
Days to Decision
90 days

PM2002 CC AND PM2002 EC

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K904948
510(k) Type
Traditional
Applicant
PLANMECA USA, INC.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
1/30/1991
Days to Decision
90 days