Points to Consider for Cervical Cytology Devices
Detailed guidance document from FDA and regulatory agencies.
Document Details
Guidance Document
July 25, 1994
March 17, 2020
8f2feffb-1a2d-4906-afa6-a031c5af0995
Related Documents
Color Additive Petitions - Medical Devices
Guidance DocumentJune 1, 1987Center for Devices and Radiological Health
Master Files Part III - Guidance on Scientific and Technical Information
Guidance DocumentJune 1, 1987Center for Devices and Radiological Health
Third Party Review Guidance for Phacofragmentation System Device Premarket Notification (510(k))
Guidance DocumentJanuary 31, 1997Center for Devices and Radiological Health
Quick Actions
Transform Regulatory Data into Actionable Intelligence
Join leading pharmaceutical and medical device companies who trust GKS for their regulatory compliance needs.
Try KeyPedia Today
Explore our real use cases and discover our features in depth.
Subscribe to our newsletter
Get the latest updates and insights delivered to your inbox