The following data is part of a premarket notification filed by Intersect Systems, Inc. with the FDA for Albumin Reagent.
Device ID | K021636 |
510k Number | K021636 |
Device Name: | ALBUMIN REAGENT |
Classification | Bromcresol Purple Dye-binding, Albumin |
Applicant | INTERSECT SYSTEMS, INC. P.O. BOX 2219 Longview, WA 98632 |
Contact | Joan Cathey |
Correspondent | Joan Cathey INTERSECT SYSTEMS, INC. P.O. BOX 2219 Longview, WA 98632 |
Product Code | CJW |
CFR Regulation Number | 862.1035 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-05-17 |
Decision Date | 2002-07-17 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00851445007006 | K021636 | 000 |