Product code LFY— Microbiology
DIASORIN LIAISON VZV IGG
- Classification name
- Enzyme Linked Immunoabsorbent Assay, Varicella-Zoster
- Device class
- Class 2
- Regulation
- 21 CFR 866.3900
- Advisory panel
- Microbiology
- Total cleared
- 17
- First cleared
- Most recent
Market context for product code LFY
FDA has cleared devices under product code LFY between 1983 and 2023, filed by 11 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 2023
- 2015
- 2007
- 2005
- 1999
- 1998
- 1997
- 1996
- 1995
- 1992
- 1990
- 1989
- 1984
- 1983
Top applicants under product code LFY
Recent clearances under product code LFY
- K231214 — LIAISON VZV IgG HT, LIAISON Control VZV IgG HT
- K150375 — LIAISON VZV IgG, LIAISON Control VZV IgG
- K070317 — ZEUS SCIENTIFIC, INC VZV IGM ELISA TEST SYSTEM
- K061820 — DIASORIN LIAISON VZV IGG
- K051484 — ZEUS SCIENTIFIC, INC., ATHENA MULTI-LYTE MMRV IGG TEST SYSTEM.
- K984181 — THE APTUS (AUTOMATED) APPLICATION OF THE VZV IGG ELISA TEST SYSTEM
- K981867 — IS-VZU IGG TEST SYSTEM
- K972295 — SERAQUEST VZV IGG
- K961012 — VZV IGG ELISA TEST SYSTEM
- K943843 — VARICELISA, MODIFICATION
- K941046 — VZV IGG ELISA TEST
- K923122 — VITEK IMMUNODIAGNOSTIC ASSAY SYSTEM
- K914022 — SERIOLOGICAL TEST KIT/IGM ANTIBODY VARI-ZOST VIRUS
- K900688 — VARICELLA ZOSTER IGG CLIN-ELISA TEST KIT
- K890642 — VZV MICROASSAY
- K833637 — VZV BIO-ENZABEAD SCREEN KIT
- K823805 — VARICELISA TEST KIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.