The following data is part of a premarket notification filed by Amsino International, Inc. with the FDA for Amsure 100% Silicone Foley Catheter.
Device ID | K051059 |
510k Number | K051059 |
Device Name: | AMSURE 100% SILICONE FOLEY CATHETER |
Classification | Catheter, Retention Type, Balloon |
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 | EZL |
CFR Regulation Number | 876.5130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-04-26 |
Decision Date | 2005-06-28 |
Summary: | summary |