Robert C. Leif, Ph.D.
Country not established
- Devices
- 1
What Robert C. Leif, Ph.D. makes
The company manufactures the LEIF Centrifugal Cytology Bucket, a device used for processing cytological samples by centrifugation to facilitate cellular analysis.
This product is classified as Class I under FDA regulations and is listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Leif Centrifugal Cytology Bucket Ref K792032
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Robert C. Leif, Ph.D. have in the registry?
The registry currently lists 1 device for Robert C. Leif, Ph.D.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Robert C. Leif, Ph.D.'s devices?
Among its 1 most recently registered device, Robert C. Leif, Ph.D. has devices listed in FDA 510(k) (1 device).
What risk classes do Robert C. Leif, Ph.D.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Robert C. Leif, Ph.D.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Robert C. Leif, Ph.D. in the registry?
The most recently registered devices listed for Robert C. Leif, Ph.D. include LEIF CENTRIFUGAL CYTOLOGY BUCKET.