The Aptus (Automated) Application of the Ebv-Vca Igg Elisa Test System. an Enzyme Linked Immunosorbent Assay (Elisa) for
K984126 is the FDA 510(k) clearance record for THE APTUS (AUTOMATED) APPLICATION OF THE EBV-VCA IGG ELISA TEST SYSTEM. AN ENZYME LINKED IMMUNOSORBENT ASSAY (ELISA) FOR, a class I device, cleared for Zeus Scientific, Inc. on under FDA product code MCD (Antigen, Ebv, Capsid). FDA records list 141 510(k) clearances for Zeus Scientific, Inc., from to . As of , FDA records show no recalls naming K984126.
Clearance record
- Decision date
- Received
- (54 days to decision)
- Product code
- MCD Antigen, Ebv, Capsid
- Regulation
- 21 CFR 866.3235
- Device class
- Class I
- Review panel
- Microbiology
- Applicant
- Zeus Scientific, Inc. 200 Evans Way, Branchburg NJ
- 510(k) summary
- Statement
- Third party review
- No
Clearances, product code MCD
Trailing 12 monthsFDA records hold no clearances under product code MCD in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
