The following data is part of a premarket notification filed by Medical Technologies, Inc. with the FDA for Cmap Pro.
Device ID | K113074 |
510k Number | K113074 |
Device Name: | CMAP PRO |
Classification | Electromyograph, Diagnostic |
Applicant | MEDICAL TECHNOLOGIES, INC. 5901-J WYOMING NE, SUITE 125 Albuquerque, NM 87106 |
Contact | Angela Morris |
Correspondent | Casey Conry UNDERWRITERS LABORATORIES, INC. 1285 WALT WHITMAN RD. Melville, NY 11747 |
Product Code | IKN |
CFR Regulation Number | 890.1375 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2011-10-17 |
Decision Date | 2012-02-02 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CMAP PRO 85171411 4226286 Dead/Cancelled |
MED-TEK LLC 2010-11-08 |