510(k) K772322
K772322 is an FDA 510(k) premarket notification submitted by Dura Corp., The for the device "DEPILATORY, ELECTRONIC". The FDA issued a decision of Substantially Equivalent on Jan 3, 1978. The device falls under product code KCX (Epilator, High Frequency, Tweezer-Type), a Class I device regulated under 21 CFR 878.5360.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jan 3, 1978
- Date Received
- Dec 19, 1977
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Epilator, High Frequency, Tweezer-Type
- Device Class
- Class I
- Regulation Number
- 878.5360
- Review Panel
- SU
- Submission Type
- 510(k) Exempt