The following data is part of a premarket notification filed by Delphi Consulting Group with the FDA for Simulscope Auscultation And Simulscope Bedside Auscultation System.
| Device ID | K961937 |
| 510k Number | K961937 |
| Device Name: | SIMULSCOPE AUSCULTATION AND SIMULSCOPE BEDSIDE AUSCULTATION SYSTEM |
| Classification | Stethoscope, Electronic |
| Applicant | DELPHI CONSULTING GROUP 11874 SOUTH EVELYN CIRCLE Houston, TX 77071 |
| Contact | J. Harvey Knauss |
| Correspondent | J. Harvey Knauss DELPHI CONSULTING GROUP 11874 SOUTH EVELYN CIRCLE Houston, TX 77071 |
| Product Code | DQD |
| CFR Regulation Number | 870.1875 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-05-20 |
| Decision Date | 1996-12-09 |
| Summary: | summary |