The following data is part of a premarket notification filed by San Cheong Co. Ltd. with the FDA for Portable Oxygen Unit Sca900.
Device ID | K080243 |
510k Number | K080243 |
Device Name: | PORTABLE OXYGEN UNIT SCA900 |
Classification | Regulator, Pressure, Gas Cylinder |
Applicant | SAN CHEONG CO. LTD. 13340 E FIRESTONE BLVD SUITE J Santa Fe Springs, CA 90670 |
Contact | Jung Bae Bang |
Correspondent | Jung Bae Bang SAN CHEONG CO. LTD. 13340 E FIRESTONE BLVD SUITE J Santa Fe Springs, CA 90670 |
Product Code | CAN |
CFR Regulation Number | 868.2700 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-01-31 |
Decision Date | 2009-04-07 |
Summary: | summary |