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PRECISEPLAN 2.0

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022411
510(k) Type
Traditional
Applicant
PRECISION THERAPY INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/20/2002
Days to Decision
58 days
Submission Type
Summary

PRECISEPLAN 2.0

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022411
510(k) Type
Traditional
Applicant
PRECISION THERAPY INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/20/2002
Days to Decision
58 days
Submission Type
Summary