The following data is part of a premarket notification filed by Vortran Medical Technology 1, Inc. with the FDA for Soft-mist(tm).
Device ID | K924649 |
510k Number | K924649 |
Device Name: | SOFT-MIST(TM) |
Classification | Nebulizer (direct Patient Interface) |
Applicant | VORTRAN MEDICAL TECHNOLOGY 1, INC. 3941 J STREET, SUITE 354 Sacramento, CA 95819 |
Contact | Gordon A Wong |
Correspondent | Gordon A Wong VORTRAN MEDICAL TECHNOLOGY 1, INC. 3941 J STREET, SUITE 354 Sacramento, CA 95819 |
Product Code | CAF |
CFR Regulation Number | 868.5630 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-09-15 |
Decision Date | 1993-05-17 |