ULTRABLADE— 510(k) K921167

Substantially Equivalent

Micron Technology, Inc.

FDA 510(k) clearance K921167 for ULTRABLADE, Substantially Equivalent on 1992-07-30. Applicant: Micron Technology, Inc.. Device class: 1.

Clearance details

Applicant: Micron Technology, Inc.
Product code: Code GDX
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1992-03-11
Decision date: 1992-07-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boulder, CO, US

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