Product code FHP— Gastroenterology, Urology
ENDOPATH VERESS NEEDLE
- Classification name
- Needle, Pneumoperitoneum, Simple
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code FHP
FDA has cleared devices under product code FHP between 1986 and 1991, filed by 2 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 1991
- 1986
Top applicants under product code FHP
Recent clearances under product code FHP
Data sourced from openFDA. This site is unofficial and independent of the FDA.