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PRECISEPLAN 2.0

Page Type
Cleared 510(K)
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)
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