MOBETRON— 510(k) K981112

Substantially Equivalent

Intraop Medical, Inc.

FDA 510(k) clearance K981112 for MOBETRON, Substantially Equivalent on 1998-07-24. Applicant: Intraop Medical, Inc..

Clearance details

Applicant: Intraop Medical, Inc.
Product code: Code LHN
Advisory panel: Radiology
Date received: 1998-03-26
Decision date: 1998-07-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Clara, CA, US

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