The following data is part of a premarket notification filed by Alba Bioscience Limited (doing Business As Quotient) with the FDA for Quality Control Kits For Blood Banking Reagents.
Device ID | BK100005 |
510k Number | BK100005 |
Device Name: | Quality Control Kits For Blood Banking Reagents |
Classification | Kit, Quality Control For Blood Banking Reagents |
Applicant | ALBA Bioscience Limited (doing Business As Quotient) 21 Ellen's Glen Road liberton, Edinburgh Scotland, United Kingdom, EH17 7QT, UK |
Product Code | KSF |
CFR Regulation Number | 864.9650 [🔎] |
Decision | Substantially Equivalent (SE) |
Type | 510(k) Traditio |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-02-17 |
Decision Date | 2010-08-26 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
05060242471162 | BK100005 | 0 |