Home › BIOCYTECH CORPORATION SDN. BHD. › PathTezt®
PathTezt®
BIOCYTECH CORPORATION SDN. BHD. · Model DF-2508 · UDI-DI 09551020410313
5
510(k) clearances
4
Adverse events
0
Recalls
57
Facilities
Description
The specimen is poured onto the dual filter, where suction removes debris at the first layer and retains cells on the second layer for slide transfer.
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
