The following data is part of a premarket notification filed by Adac Laboratories with the FDA for Autospect Plus With Instill Motion Correction.
| Device ID | K992317 |
| 510k Number | K992317 |
| Device Name: | AUTOSPECT PLUS WITH INSTILL MOTION CORRECTION |
| Classification | System, Tomography, Computed, Emission |
| Applicant | ADAC LABORATORIES 540 ALDER DR. Milpitas, CA 95035 |
| Contact | Dennis W Henkelman |
| Correspondent | Dennis W Henkelman ADAC LABORATORIES 540 ALDER DR. Milpitas, CA 95035 |
| Product Code | KPS |
| CFR Regulation Number | 892.1200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-07-09 |
| Decision Date | 1999-10-01 |
| Summary: | summary |