FDA Device Establishments · JSON-LD · Markdown

CytoTest, Inc.

FEI 3008849407 · Manufacture Medical Device · Status: Active

FEI Number3008849407
Owner / OperatorCytoTest, Inc. (#10035058)
Address1395 Piccard Drive, Ste. 308, Rockville, MD, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)MVU
Regulation § (21 CFR)864.4020
Proprietary namesELN/CUX1 FISH Probe Kit; LSP TCF3 5' FISH Probe; SRY/CCPX FISH Probe Kit; SNRPN/PML FISH Probe Kit; MNX1 Break Apart FISH Probe Kit; NCOA4-RET Fusion/Translocation FISH Probe Kit; LSP NF2 FISH Probe; NTRK1,2,3 Break Apart FISH Probe Kit; S100A10/PNOC FISH Probe Kit; LSP D7S522 FISH Probe

External sources

Source: openFDA. Public-domain (CC0).