The following data is part of a premarket notification filed by Orion Corp. with the FDA for Chlamyset Antibody Eia.
Device ID | K864457 |
510k Number | K864457 |
Device Name: | CHLAMYSET ANTIBODY EIA |
Classification | Enzyme Linked Immunoabsorbent Assay, (chlamydiae Group) |
Applicant | ORION CORP. P.O. BOX 425 20101 Turku, FI |
Contact | Timo Raines |
Correspondent | Timo Raines ORION CORP. P.O. BOX 425 20101 Turku, FI |
Product Code | LJC |
CFR Regulation Number | 866.3120 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-11-12 |
Decision Date | 1987-09-11 |