The following data is part of a premarket notification filed by Bayer Healthcare Llc with the FDA for Contour Next Blood Glucose Meter.
Device ID | K121190 |
510k Number | K121190 |
Device Name: | CONTOUR NEXT BLOOD GLUCOSE METER |
Classification | Glucose Dehydrogenase, Glucose |
Applicant | BAYER HEALTHCARE LLC 555 WHITE PLAINS RD. Tarrytown, NY 10591 |
Contact | Charles Ryan |
Correspondent | Charles Ryan BAYER HEALTHCARE LLC 555 WHITE PLAINS RD. Tarrytown, NY 10591 |
Product Code | LFR |
Subsequent Product Code | JJX |
Subsequent Product Code | NBW |
CFR Regulation Number | 862.1345 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-04-19 |
Decision Date | 2012-07-26 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
40301939697018 | K121190 | 000 |
40301937278707 | K121190 | 000 |
50301937314013 | K121190 | 000 |
50301937315010 | K121190 | 000 |
40301937308503 | K121190 | 000 |
40301937357501 | K121190 | 000 |
40301939735253 | K121190 | 000 |
40301939736502 | K121190 | 000 |
40301939737219 | K121190 | 000 |
10301937313100 | K121190 | 000 |
40301937283350 | K121190 | 000 |
40301937377011 | K121190 | 000 |
40301937379015 | K121190 | 000 |
40301937277359 | K121190 | 000 |