The following data is part of a premarket notification filed by Pharmacia Diagnostics Ab with the FDA for Modification To: Unicap Specific Ige.
Device ID | K051218 |
510k Number | K051218 |
Device Name: | MODIFICATION TO: UNICAP SPECIFIC IGE |
Classification | System, Test, Radioallergosorbent (rast) Immunological |
Applicant | PHARMACIA DIAGNOSTICS AB 4169 COMMERCIAL AVENUE Portage, MI 49002 |
Contact | Martin R Mann |
Correspondent | Martin R Mann PHARMACIA DIAGNOSTICS AB 4169 COMMERCIAL AVENUE Portage, MI 49002 |
Product Code | DHB |
CFR Regulation Number | 866.5750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-05-12 |
Decision Date | 2005-06-09 |
Summary: | summary |