The following data is part of a premarket notification filed by Derma Media Lab., Inc. with the FDA for Albumin.
| Device ID | K955781 |
| 510k Number | K955781 |
| Device Name: | ALBUMIN |
| Classification | Bromcresol Green Dye-binding, Albumin |
| Applicant | DERMA MEDIA LAB., INC. 8531 WELLSFORD PL., SUITE E Santa Fe Springs, CA 90670 |
| Contact | Charles C Allain |
| Correspondent | Charles C Allain DERMA MEDIA LAB., INC. 8531 WELLSFORD PL., SUITE E Santa Fe Springs, CA 90670 |
| Product Code | CIX |
| CFR Regulation Number | 862.1035 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-12-21 |
| Decision Date | 1996-03-13 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00851445007013 | K955781 | 000 |