MEC-I-TRON, MODEL P-1— 510(k) K873190

Name: FDA 510(k) clearance K873190
Creator: U.S. Food and Drug Administration
Published: 1987-12-18

Substantially Equivalent

Meyer Equipment Company, Inc.

FDA 510(k) clearance K873190 for MEC-I-TRON, MODEL P-1, Substantially Equivalent on 1987-12-18. Applicant: Meyer Equipment Company, Inc.. Device class: 2.

Clearance details

Applicant: Meyer Equipment Company, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1987-08-13
Decision date: 1987-12-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lee'S Summit, MO, US

Download summary PDF View on FDA.gov ↗

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