PRECISEPLAN 2.0— 510(k) K022411

Substantially Equivalent

Precision Therapy Intl., Inc.

FDA 510(k) clearance K022411 for PRECISEPLAN 2.0, Substantially Equivalent on 2002-09-20. Applicant: Precision Therapy Intl., Inc..

Clearance details

Applicant: Precision Therapy Intl., Inc.
Product code: Code MUJ
Advisory panel: Radiology
Date received: 2002-07-24
Decision date: 2002-09-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norcross, GA, US

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