The following data is part of a premarket notification filed by Microscan Div. Baxter Healthcare Corp. with the FDA for Antibody Assay For Detection Of Adenovirus In Cell.
Device ID | K871229 |
510k Number | K871229 |
Device Name: | ANTIBODY ASSAY FOR DETECTION OF ADENOVIRUS IN CELL |
Classification | Antigens, Cf (including Cf Control), Adenovirus 1-33 |
Applicant | MICROSCAN DIV. BAXTER HEALTHCARE CORP. 2040 ENTERPRISE BLVD. W. Sacramento, CA 95691 |
Contact | Howard G Taylor |
Correspondent | Howard G Taylor MICROSCAN DIV. BAXTER HEALTHCARE CORP. 2040 ENTERPRISE BLVD. W. Sacramento, CA 95691 |
Product Code | GOD |
CFR Regulation Number | 866.3020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-03-27 |
Decision Date | 1987-06-26 |