The following data is part of a premarket notification filed by Hollister, Inc. with the FDA for Anal 2 Electrode Stimulation/emg Probe - W/stop.
| Device ID | K990456 |
| 510k Number | K990456 |
| Device Name: | ANAL 2 ELECTRODE STIMULATION/EMG PROBE - W/STOP |
| Classification | Stimulator, Electrical, Non-implantable, For Incontinence |
| Applicant | HOLLISTER, INC. 2000 HOLLISTER DR. Libertyville, IL 60048 |
| Contact | Joseph S Tokarz |
| Correspondent | Joseph S Tokarz HOLLISTER, INC. 2000 HOLLISTER DR. Libertyville, IL 60048 |
| Product Code | KPI |
| CFR Regulation Number | 876.5320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-02-12 |
| Decision Date | 1999-03-25 |
| Summary: | summary |