The following data is part of a premarket notification filed by Persyst Development Corporation with the FDA for Persyst 13 (p13) Eeg Review And Analysis Software.
| Device ID | K151929 |
| 510k Number | K151929 |
| Device Name: | PERSYST 13 (P13) EEG REVIEW AND ANALYSIS SOFTWARE |
| Classification | Automatic Event Detection Software For Full-montage Electroencephalograph |
| Applicant | PERSYST DEVELOPMENT CORPORATION 12625 HIGH BLUFF DRIVE, SUITE 213 San Diego, CA 92130 |
| Contact | Dari Darabbeigi |
| Correspondent | Dari Darabbeigi PERSYST DEVELOPMENT CORPORATION 12625 HIGH BLUFF DRIVE, SUITE 213 San Diego, CA 92130 |
| Product Code | OMB |
| Subsequent Product Code | OLT |
| Subsequent Product Code | OMA |
| CFR Regulation Number | 882.1400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-07-14 |
| Decision Date | 2015-08-12 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00869732000111 | K151929 | 000 |