The following data is part of a premarket notification filed by B & B Medical Technologies, Inc. with the FDA for Bodai M.d.d. Adaptor(tm).
Device ID | K881849 |
510k Number | K881849 |
Device Name: | BODAI M.D.D. ADAPTOR(TM) |
Classification | Connector, Airway (extension) |
Applicant | B & B MEDICAL TECHNOLOGIES, INC. 3569 RECYCLE RD., SUITE 16 Rancho Cordova, CA 95670 |
Contact | W Briggs,iii |
Correspondent | W Briggs,iii B & B MEDICAL TECHNOLOGIES, INC. 3569 RECYCLE RD., SUITE 16 Rancho Cordova, CA 95670 |
Product Code | BZA |
CFR Regulation Number | 868.5810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-05-02 |
Decision Date | 1988-07-01 |