The following data is part of a premarket notification filed by Amsino Intl., Inc. with the FDA for Amsino Suction Catheter.
| Device ID | K973199 |
| 510k Number | K973199 |
| Device Name: | AMSINO SUCTION CATHETER |
| Classification | Catheters, Suction, Tracheobronchial |
| Applicant | AMSINO INTL., INC. 833 TOWNE CENTER DR. Pomona, CA 91767 |
| Contact | Richard Y Li |
| Correspondent | Richard Y Li AMSINO INTL., INC. 833 TOWNE CENTER DR. Pomona, CA 91767 |
| Product Code | BSY |
| CFR Regulation Number | 868.6810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-08-26 |
| Decision Date | 1997-09-10 |