The following data is part of a premarket notification filed by K & S Medicorp with the FDA for Saltzman Stethoscope Head.
| Device ID | K854771 |
| 510k Number | K854771 |
| Device Name: | SALTZMAN STETHOSCOPE HEAD |
| Classification | Stethoscope, Manual |
| Applicant | K & S MEDICORP 7860 S.W. 147 ST. Miami, FL 33158 |
| Contact | Saltzman Md |
| Correspondent | Saltzman Md K & S MEDICORP 7860 S.W. 147 ST. Miami, FL 33158 |
| Product Code | LDE |
| CFR Regulation Number | 870.1875 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-11-29 |
| Decision Date | 1986-05-09 |