DMI 250 SERIES POWER SURGERY TABLE— 510(k) K894789

Name: FDA 510(k) clearance K894789
Creator: U.S. Food and Drug Administration
Published: 1989-08-29

Substantially Equivalent

M.D. Intl., Inc.

FDA 510(k) clearance K894789 for DMI 250 SERIES POWER SURGERY TABLE, Substantially Equivalent on 1989-08-29. Applicant: M.D. Intl., Inc.. Device class: 1.

Clearance details

Applicant: M.D. Intl., Inc.
Product code: Code JEA
Device class: Class 1
Regulation: 21 CFR 878.4960
Advisory panel: General, Plastic Surgery
Date received: 1989-07-28
Decision date: 1989-08-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.