The following data is part of a premarket notification filed by Inova Diagnostics, Inc. with the FDA for Quanta Plex Sle Profile 8.
Device ID | K040160 |
510k Number | K040160 |
Device Name: | QUANTA PLEX SLE PROFILE 8 |
Classification | Extractable Antinuclear Antibody, Antigen And Control |
Applicant | INOVA DIAGNOSTICS, INC. 10180 SCRIPPS RANCH BLVD. San Diego, CA 92131 |
Contact | Brys C Myers |
Correspondent | Brys C Myers INOVA DIAGNOSTICS, INC. 10180 SCRIPPS RANCH BLVD. San Diego, CA 92131 |
Product Code | LLL |
CFR Regulation Number | 866.5100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-01-23 |
Decision Date | 2004-03-08 |