Product code KYH— Gastroenterology, Urology
GM OPTI*CAM CAMERA WITH FIBER OPTIC LIGHT
- Classification name
- Endoscope, Ophthalmic
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code KYH
FDA has cleared device under product code KYH, all in 1994, 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 KYH
Recent clearances under product code KYH
Data sourced from openFDA. This site is unofficial and independent of the FDA.