PROMATRON 3000— 510(k) K901566

Substantially Equivalent

Promatek Medical Systems, Inc.

FDA 510(k) clearance K901566 for PROMATRON 3000, Substantially Equivalent on 1990-10-29. Applicant: Promatek Medical Systems, Inc.. Device class: 2.

Clearance details

Applicant: Promatek Medical Systems, Inc.
Product code: Code IKK
Device class: Class 2
Regulation: 21 CFR 890.1925
Advisory panel: Physical Medicine
Date received: 1990-04-03
Decision date: 1990-10-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Joliet, IL, US

Download summary PDF View on FDA.gov ↗

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