DMI SERIES 90 EXAMINATION TABLE— 510(k) K894788

Name: FDA 510(k) clearance K894788
Creator: U.S. Food and Drug Administration
Published: 1989-09-08

Substantially Equivalent

M.D. Intl., Inc.

FDA 510(k) clearance K894788 for DMI SERIES 90 EXAMINATION TABLE, Substantially Equivalent on 1989-09-08. Applicant: M.D. Intl., Inc.. Device class: 1.

Clearance details

Applicant: M.D. Intl., Inc.
Product code: Code KMN
Device class: Class 1
Regulation: 21 CFR 880.6140
Advisory panel: General Hospital
Date received: 1989-07-28
Decision date: 1989-09-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

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