The following data is part of a premarket notification filed by Shield Diagnostics, Ltd. with the FDA for Diastat Anti-nuclear Antibody (ana) Kit.
Device ID | K932876 |
510k Number | K932876 |
Device Name: | DIASTAT ANTI-NUCLEAR ANTIBODY (ANA) KIT |
Classification | Antinuclear Antibody, Antigen, Control |
Applicant | SHIELD DIAGNOSTICS, LTD. THE TECHNOLOGY PARK Dundee, GB Dd2 1sw |
Contact | George Zajicek |
Correspondent | George Zajicek SHIELD DIAGNOSTICS, LTD. THE TECHNOLOGY PARK Dundee, GB Dd2 1sw |
Product Code | LKJ |
CFR Regulation Number | 866.5100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-06-14 |
Decision Date | 1993-11-15 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
07340058410486 | K932876 | 000 |