The following data is part of a premarket notification filed by Bionostics, Inc. with the FDA for Lifescan Onetouch Select / Ultra / Vita Glucose Control Solution.
| Device ID | K103553 |
| 510k Number | K103553 |
| Device Name: | LIFESCAN ONETOUCH SELECT / ULTRA / VITA GLUCOSE CONTROL SOLUTION |
| Classification | Single (specified) Analyte Controls (assayed And Unassayed) |
| Applicant | BIONOSTICS, INC. 7 JACKSON RD. Devens, MA 01434 |
| Contact | Randy Byrd |
| Correspondent | Randy Byrd BIONOSTICS, INC. 7 JACKSON RD. Devens, MA 01434 |
| Product Code | JJX |
| CFR Regulation Number | 862.1660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-12-03 |
| Decision Date | 2011-02-10 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20353885006235 | K103553 | 000 |
| 20353885458027 | K103553 | 000 |