![FDA, FTC and DOJ Enforcement of Medical Device Regulations FDA, FTC and DOJ Enforcement of Medical Device Regulations](https://www.fdanews.com/ext/resources/Book-Covers-2/BFFDEMDR-COVER.png?height=200&t=1685733565&width=200)
Home » DIAMICS SUBMITS 510K TO FDA FOR UNIQUE CERVICAL COLLECTION DEVICE
DIAMICS SUBMITS 510K TO FDA FOR UNIQUE CERVICAL COLLECTION DEVICE
Diamics, Inc., a San Francisco Bay-area, medical device and diagnostics company, announced it has submitted a 510(k) premarket notification application to the FDA for its proprietary CerCol cervical collection device. The CerCol device
is designed to improve screening for cervical cancer and greater comfort to
the patient.
Yahoo
News
KEYWORDS FDAnews Device Daily Bulletin
Upcoming Events
-
21Oct