Advanced Cytometrix, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Advanced Cytometrix, Inc. makes
Advanced Cytometrix, Inc. manufactures biopsy tools for medical diagnostics, including single-lumen biopsy needles, fine needle aspiration biopsy kits, and a pulsating vacuum pump system designed to assist in tissue sampling procedures.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Aci Single Lumen Biopsy Needle Ref K954264
Regimes: 510(k) Registry: 510(k)Aci Pulsating Vacuum Pump System Ref K954286
Regimes: 510(k) Registry: 510(k)Aci Fine Needle Aspiration Biopsy Kit Ref K954287
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Advanced Cytometrix, Inc. have in the registry?
The registry currently lists 3 devices for Advanced Cytometrix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Advanced Cytometrix, Inc.'s devices?
Among its 3 most recently registered devices, Advanced Cytometrix, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Advanced Cytometrix, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Advanced Cytometrix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Advanced Cytometrix, Inc. in the registry?
The most recently registered devices listed for Advanced Cytometrix, Inc. include ACI SINGLE LUMEN BIOPSY NEEDLE, ACI PULSATING VACUUM PUMP SYSTEM and ACI FINE NEEDLE ASPIRATION BIOPSY KIT.