The following data is part of a premarket notification filed by Bbi Diagnostics, A Seracare Company with the FDA for Single (specified) Analyte Controls, (assayed And Unassayed).
Device ID | BK040064 |
510k Number | BK040064 |
Device Name: | Single (Specified) Analyte Controls, (Assayed And Unassayed) |
Classification | Single (specified) Analyte Controls (assayed And Unassayed) |
Applicant | BBI Diagnostics, A SeraCare Company 375 West Street West Bridgewater, MA 02379 |
Product Code | JJX |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SE) |
Type | 510(k) Traditio |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-08-02 |
Decision Date | 2004-10-29 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00816784020628 | BK040064 | 0 |
00816784020611 | BK040064 | 0 |
00816784020604 | BK040064 | 0 |
00816784020598 | BK040064 | 0 |
00816784020581 | BK040064 | 0 |