MULTISCOPE
Stethoscope, Electronic
AMDIA MEDICAL PRODUCTS
The following data is part of a premarket notification filed by Amdia Medical Products with the FDA for Multiscope.
Pre-market Notification Details
| Device ID | K791334 |
| 510k Number | K791334 |
| Device Name: | MULTISCOPE |
| Classification | Stethoscope, Electronic |
| Applicant | AMDIA MEDICAL PRODUCTS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DQD |
| CFR Regulation Number | 870.1875 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-07-20 |
| Decision Date | 1979-08-10 |
Trademark Results [MULTISCOPE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MULTISCOPE 78446946 2992336 Live/Registered |
Zibra Corporation 2004-07-07 |
 MULTISCOPE 78001084 not registered Dead/Abandoned |
Wittig Test Technology GmbH 2000-03-27 |
 MULTISCOPE 75476145 2538476 Live/Registered |
FLIR COMMERCIAL SYSTEMS, INC. 1998-04-28 |
 MULTISCOPE 73828207 1649321 Dead/Cancelled |
LOGITECH INC. 1989-08-21 |
 MULTISCOPE 71589626 0551926 Dead/Expired |
BINGHAM-HERBRAND CORPORATION, THE 1949-12-20 |
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