The following data is part of a premarket notification filed by Doodlebug Products, Llc with the FDA for Barf Band.
| Device ID | K110821 |
| 510k Number | K110821 |
| Device Name: | BARF BAND |
| Classification | Device, Acupressure |
| Applicant | DOODLEBUG PRODUCTS, LLC 5 HEMINGWAY LANE West Newbury, MA 01985 |
| Contact | Barry E Sands |
| Correspondent | Barry E Sands DOODLEBUG PRODUCTS, LLC 5 HEMINGWAY LANE West Newbury, MA 01985 |
| Product Code | MVV |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-03-24 |
| Decision Date | 2012-02-27 |
| Summary: | summary |