The following data is part of a premarket notification filed by Becton Dickinson & Co. with the FDA for Bd Alcohol Swab.
Device ID | K121655 |
510k Number | K121655 |
Device Name: | BD ALCOHOL SWAB |
Classification | Pad, Alcohol, Device Disinfectant |
Applicant | BECTON DICKINSON & CO. 1 BECTON DR. Franklin Lakes, NJ 07417 -1885 |
Contact | Avital Lakes |
Correspondent | Avital Lakes BECTON DICKINSON & CO. 1 BECTON DR. Franklin Lakes, NJ 07417 -1885 |
Product Code | LKB |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-06-05 |
Decision Date | 2013-03-20 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
50382903065597 | K121655 | 000 |
50382903065580 | K121655 | 000 |
50382903065573 | K121655 | 000 |