OMNIVISION

System, Image Processing, Radiological

MODERN MODULE INC

The following data is part of a premarket notification filed by Modern Module Inc with the FDA for Omnivision.

Pre-market Notification Details

• Device ID: K110040
• 510k Number: K110040
• Device Name: OMNIVISION
• Classification: System, Image Processing, Radiological
• Applicant: MODERN MODULE INC 425 CHEONGCHUN-DONG, BUPYUNG-KU Lncheon, KR
• Contact: Samuel Koh
• Correspondent: Marc M Mouser; UNDERWRITERS LABORATORIES, INC. 2600 NW LAKE RD. Camas, WA 98607 -9526
• Product Code: LLZ
• CFR Regulation Number: 892.2050 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: Yes
• Combination Product: No
• Date Received: 2011-01-06
• Decision Date: 2011-01-26
• Summary: summary