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PM2002 PROLINE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923534
510(k) Type
Traditional
Applicant
PLANMECA USA, INC.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
1/31/1994
Days to Decision
564 days
Submission Type
Statement

PM2002 PROLINE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923534
510(k) Type
Traditional
Applicant
PLANMECA USA, INC.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
1/31/1994
Days to Decision
564 days
Submission Type
Statement