MICROPHOR

Device, Iontophoresis, Other Uses

LIFE-TECH INTL., INC.

The following data is part of a premarket notification filed by Life-tech Intl., Inc. with the FDA for Microphor.

Pre-market Notification Details

• Device ID: K913601
• 510k Number: K913601
• Device Name: MICROPHOR
• Classification: Device, Iontophoresis, Other Uses
• Applicant: LIFE-TECH INTL., INC. P.O. BOX 36221 Houston, TX 77236 -6221
• Contact: Alfred C Coats
• Correspondent: Alfred C Coats; LIFE-TECH INTL., INC. P.O. BOX 36221 Houston, TX 77236 -6221
• Product Code: EGJ
• CFR Regulation Number: 890.5525 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1991-08-13
• Decision Date: 1994-07-15