Product code HPO— Ophthalmic
DORC INTRAOCULAR ELECTROMAGNET
- Classification name
- Magnet, Ac-Powered
- Device class
- Class 2
- Regulation
- 21 CFR 886.4440
- Advisory panel
- Ophthalmic
- Total cleared
- 3
- First cleared
- Most recent
Market context for product code HPO
FDA has cleared devices under product code HPO between 1983 and 1986, filed by 3 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
- 1986
- 1983
Top applicants under product code HPO
Recent clearances under product code HPO
Data sourced from openFDA. This site is unofficial and independent of the FDA.