The following data is part of a premarket notification filed by Amdia Medical Products with the FDA for Nursescope.
| Device ID | K791335 | 
| 510k Number | K791335 | 
| Device Name: | NURSESCOPE | 
| 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 | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  NURSESCOPE  72221466  0804793 Dead/Expired | CARDIOSONICS MEDICAL INSTRUMENTS CORPORATION 1965-06-18 |