The following data is part of a premarket notification filed by Amsino International, Inc. with the FDA for Amsino Endotracheal Tube.
Device ID | K050785 |
510k Number | K050785 |
Device Name: | AMSINO ENDOTRACHEAL TUBE |
Classification | Tube, Tracheal (w/wo Connector) |
Applicant | AMSINO INTERNATIONAL, INC. 855 TOWNE CENTER DRIVE Pomona, CA 91767 |
Contact | Ching Ching Seah |
Correspondent | Ching Ching Seah AMSINO INTERNATIONAL, INC. 855 TOWNE CENTER DRIVE Pomona, CA 91767 |
Product Code | BTR |
CFR Regulation Number | 868.5730 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-03-28 |
Decision Date | 2005-07-15 |