The following data is part of a premarket notification filed by Roche Diagnostics with the FDA for Beta-crosslaps Calcheck 5.
| Device ID | K170678 |
| 510k Number | K170678 |
| Device Name: | Beta-CrossLaps CalCheck 5 |
| Classification | Single (specified) Analyte Controls (assayed And Unassayed) |
| Applicant | Roche Diagnostics 9115 Hague Road Indianapolis, IN 46250 |
| Contact | Edie Brunt |
| Correspondent | Edie Brunt Roche Diagnostics 9115 Hague Road Indianapolis, IN 46250 |
| Product Code | JJX |
| CFR Regulation Number | 862.1660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-03-06 |
| Decision Date | 2017-04-04 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 07613336143162 | K170678 | 000 |