The following data is part of a premarket notification filed by Elscint, Inc. with the FDA for Select/sp.
| Device ID | K961464 |
| 510k Number | K961464 |
| Device Name: | SELECT/SP |
| Classification | System, X-ray, Tomography, Computed |
| Applicant | ELSCINT, INC. 505 MAIN ST. SUITE 300 Hackensack, NJ 07601 |
| Contact | Thomas J Spackman, M.d., F.a.c.r. |
| Correspondent | Thomas J Spackman, M.d., F.a.c.r. ELSCINT, INC. 505 MAIN ST. SUITE 300 Hackensack, NJ 07601 |
| Product Code | JAK |
| CFR Regulation Number | 892.1750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-04-17 |
| Decision Date | 1996-07-03 |
| Summary: | summary |