MAGNESIUM

Photometric Method, Magnesium

TECH-CO, INC.

The following data is part of a premarket notification filed by Tech-co, Inc. with the FDA for Magnesium.

Pre-market Notification Details

• Device ID: K874847
• 510k Number: K874847
• Device Name: MAGNESIUM
• Classification: Photometric Method, Magnesium
• Applicant: TECH-CO, INC. 24111 BEVERLY Oak Park, MI 48237
• Contact: Happy Chen
• Correspondent: Happy Chen; TECH-CO, INC. 24111 BEVERLY Oak Park, MI 48237
• Product Code: JGJ
• CFR Regulation Number: 862.1495 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1987-11-24
• Decision Date: 1987-12-18

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
10673486002126	K874847	000
10673486002096	K874847	000