ULTRABLADE

Scalpel, One-piece

MICRON TECHNOLOGY, INC.

The following data is part of a premarket notification filed by Micron Technology, Inc. with the FDA for Ultrablade.

Pre-market Notification Details

• Device ID: K921167
• 510k Number: K921167
• Device Name: ULTRABLADE
• Classification: Scalpel, One-piece
• Applicant: MICRON TECHNOLOGY, INC. CENTENNIAL CREEK OFFICE PARK 2975 VALMONT AVE., SUITE 310 Boulder, CO 80301
• Contact: Richard Rosenthal
• Correspondent: Richard Rosenthal; MICRON TECHNOLOGY, INC. CENTENNIAL CREEK OFFICE PARK 2975 VALMONT AVE., SUITE 310 Boulder, CO 80301
• Product Code: GDX
• CFR Regulation Number: 878.4800 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1992-03-11
• Decision Date: 1992-07-30