The following data is part of a premarket notification filed by Biowhittaker Molecular Applications, Inc. with the FDA for Varicelisa, Modification.
Device ID | K943843 |
510k Number | K943843 |
Device Name: | VARICELISA, MODIFICATION |
Classification | Enzyme Linked Immunoabsorbent Assay, Varicella-zoster |
Applicant | BIOWHITTAKER MOLECULAR APPLICATIONS, INC. 8830 BIGGS FORD RD. Walkersville, MD 21793 -0127 |
Contact | Leif E Olsen |
Correspondent | Leif E Olsen BIOWHITTAKER MOLECULAR APPLICATIONS, INC. 8830 BIGGS FORD RD. Walkersville, MD 21793 -0127 |
Product Code | LFY |
CFR Regulation Number | 866.3900 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-07-28 |
Decision Date | 1996-03-14 |