MINI-LOGGER SERIES 2000— 510(k) K991045

Substantially Equivalent

Mini-Mitter Co., Inc.

FDA 510(k) clearance K991045 for MINI-LOGGER SERIES 2000, Substantially Equivalent on 1999-09-21. Applicant: Mini-Mitter Co., Inc.. Device class: 2.

Clearance details

Applicant: Mini-Mitter Co., Inc.
Product code: Code GWK
Device class: Class 2
Regulation: 21 CFR 882.1845
Advisory panel: Neurology
Date received: 1999-03-29
Decision date: 1999-09-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sunriver, OR, US

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