Product code HHP— Obstetrics/Gynecology
TENET MLTI-POSITIONING SURGICAL STIRRUP SYSTEM
- Classification name
- Table, Obstetrical, Manual (And Accessories)
- Device class
- Class 2
- Regulation
- 21 CFR 884.4900
- Advisory panel
- Obstetrics/Gynecology
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code HHP
FDA has cleared devices under product code HHP between 1982 and 1997, 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
- 1997
- 1982
Top applicants under product code HHP
Recent clearances under product code HHP
Data sourced from openFDA. This site is unofficial and independent of the FDA.