510(k) K770943
- Device
- Endoscope, Urological, Female
- Applicant
- C.R. BARD, INC.
- 510(k) number
- K770943
- Product code
- FAL
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-10-18
- Date received
- 1977-05-25
- Regulation
- 876.1500
- Classification name
- Panendoscope (Urethroscope)
- Medical specialty
- Gastroenterology, Urology
- Review panel
- Gastroenterology, Urology
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- N
Related Records
Applicant Contact
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
Source Documents
510(k) summary PDF not indicated by FDA