Product code GZQ— Neurology
FUJITENS III
- Classification name
- Instrument, Dowel Cutting
- Device class
- Class 2
- Regulation
- 21 CFR 882.4275
- Advisory panel
- Neurology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code GZQ
FDA has cleared device under product code GZQ, all in 1989, filed by 1 applicant company. 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.
Top applicants under product code GZQ
Recent clearances under product code GZQ
Data sourced from openFDA. This site is unofficial and independent of the FDA.