The following data is part of a premarket notification filed by Coloplast A/s with the FDA for Peristeen Anal Irrigation System, Peristeen Anal Irrigation Accessory Unit, Peristeen Anal Irrigation Rectal Catheter.
Device ID | K112860 |
510k Number | K112860 |
Device Name: | PERISTEEN ANAL IRRIGATION SYSTEM, PERISTEEN ANAL IRRIGATION ACCESSORY UNIT, PERISTEEN ANAL IRRIGATION RECTAL CATHETER |
Classification | Tubes, Gastrointestinal (and Accessories) |
Applicant | COLOPLAST A/S 1601 WEST RIVER ROAD NORTH Minneapolis, MN 55411 |
Contact | Brian Schmidt |
Correspondent | Brian Schmidt COLOPLAST A/S 1601 WEST RIVER ROAD NORTH Minneapolis, MN 55411 |
Product Code | KNT |
CFR Regulation Number | 876.5980 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-09-30 |
Decision Date | 2012-06-08 |
Summary: | summary |