The following data is part of a premarket notification filed by Hudson Oxygen Therapy Sales Co. with the FDA for Mdi Adaptor.
Device ID | K900783 |
510k Number | K900783 |
Device Name: | MDI ADAPTOR |
Classification | Nebulizer (direct Patient Interface) |
Applicant | HUDSON OXYGEN THERAPY SALES CO. 27711 DIAZ ST. P.O. BOX 66 Temecula, CA 92390 |
Contact | Jorge Haider |
Correspondent | Jorge Haider HUDSON OXYGEN THERAPY SALES CO. 27711 DIAZ ST. P.O. BOX 66 Temecula, CA 92390 |
Product Code | CAF |
CFR Regulation Number | 868.5630 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-02-20 |
Decision Date | 1990-07-18 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
14026704595546 | K900783 | 000 |
24026704656930 | K900783 | 000 |
24026704595543 | K900783 | 000 |
24026704595093 | K900783 | 000 |
24026704390223 | K900783 | 000 |