The following data is part of a premarket notification filed by 3m Company with the FDA for 3m Liquid Bandage.
Device ID | K053409 |
510k Number | K053409 |
Device Name: | 3M LIQUID BANDAGE |
Classification | Bandage, Liquid |
Applicant | 3M COMPANY 3M CENTER, BLDG. 275-5W-06 St. Paul, MN 55144 -1000 |
Contact | Bryan Becker |
Correspondent | Bryan Becker 3M COMPANY 3M CENTER, BLDG. 275-5W-06 St. Paul, MN 55144 -1000 |
Product Code | KMF |
CFR Regulation Number | 880.5090 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-12-07 |
Decision Date | 2006-06-19 |
Summary: | summary |