Product code EMK— Dental
930/0 TO 950/6 VARIOUS TYPES OF BONE CURETTES
- Classification name
- Curette, Surgical, Dental
- Device class
- Class 1
- Regulation
- 21 CFR 872.4565
- Advisory panel
- Dental
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code EMK
FDA has cleared device under product code EMK, all in 1985, filed by 1 applicant company. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Top applicants under product code EMK
Recent clearances under product code EMK
Data sourced from openFDA. This site is unofficial and independent of the FDA.