The following data is part of a premarket notification filed by Everest & Jennings, Inc. with the FDA for Magnum.
Device ID | K904817 |
510k Number | K904817 |
Device Name: | MAGNUM |
Classification | Wheelchair, Powered |
Applicant | EVEREST & JENNINGS, INC. 3233 E MISSION OAKS BLVD. Camarillo, CA 93010 |
Contact | Jackie Wilkins |
Correspondent | Jackie Wilkins EVEREST & JENNINGS, INC. 3233 E MISSION OAKS BLVD. Camarillo, CA 93010 |
Product Code | ITI |
CFR Regulation Number | 890.3860 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-10-24 |
Decision Date | 1990-11-05 |