510(k) K180953
K180953 is an FDA 510(k) premarket notification submitted by Dms Co., Ltd. for the device "AnyCheck IMT-100". The FDA issued a decision of Substantially Equivalent on Feb 20, 2019. The device falls under product code EKX (Handpiece, Direct Drive, Ac-Powered), a Class I device regulated under 21 CFR 872.4200.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 20, 2019
- Date Received
- Apr 11, 2018
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Handpiece, Direct Drive, Ac-Powered
- Device Class
- Class I
- Regulation Number
- 872.4200
- Review Panel
- DE
- Submission Type
- 510(k)