The following data is part of a premarket notification filed by Ashai Co. Ltd. with the FDA for Maxi-neb.
Device ID | K852627 |
510k Number | K852627 |
Device Name: | MAXI-NEB |
Classification | Nebulizer, Medicinal, Non-ventilatory (atomizer) |
Applicant | ASHAI CO. LTD. 620 HARRIS ST. ULTIMO, N.S.W. 2007 Australia, AU |
Contact | Kalnin |
Correspondent | Kalnin ASHAI CO. LTD. 620 HARRIS ST. ULTIMO, N.S.W. 2007 Australia, AU |
Product Code | CCQ |
CFR Regulation Number | 868.5640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-06-20 |
Decision Date | 1985-09-26 |