UNIVERSAL EXAMINATION TABLE— 510(k) K874934

Substantially Equivalent

Imatron, Inc.

FDA 510(k) clearance K874934 for UNIVERSAL EXAMINATION TABLE, Substantially Equivalent on 1988-01-19. Applicant: Imatron, Inc.. Device class: 2.

Clearance details

Applicant
Imatron, Inc.
Product code
Code KXJ
Device class
Class 2
Regulation
21 CFR 892.1980
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
South San Fransisco, CA, US
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