FDA Device Establishments · JSON-LD · Markdown

Pentax of America, Inc.

FEI 3008780134 · Manufacture Medical Device · Status: Active

FEI Number3008780134
Owner / OperatorHOYA Corporation PENTAX Division (#8030235)
Address303 Convention Way Ste 1 Ste 3, Redwood City, CA, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)GEH
Regulation § (21 CFR)878.4350
Proprietary namesC2 CryoAblation Full 8 Catheter

External sources

Source: openFDA. Public-domain (CC0).