The following data is part of a premarket notification filed by Amsino International, Inc. with the FDA for Amself Closed Catheterization System.
| Device ID | K082831 |
| 510k Number | K082831 |
| Device Name: | AMSELF CLOSED CATHETERIZATION SYSTEM |
| Classification | Tray, Catheterization, Sterile Urethral, With Or Without Catheter (kit) |
| Applicant | AMSINO INTERNATIONAL, INC. 855 TOWNE CENTER DR. Pomona, CA 91767 |
| Contact | Ching Ching Seah |
| Correspondent | Ching Ching Seah AMSINO INTERNATIONAL, INC. 855 TOWNE CENTER DR. Pomona, CA 91767 |
| Product Code | FCM |
| CFR Regulation Number | 876.5130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-09-26 |
| Decision Date | 2008-10-23 |
| Summary: | summary |