510(k) K861772
K861772 is an FDA 510(k) premarket notification submitted by Pacific Poly Crafts for the device "LASER SKIN MARKER AND MASK WHITE LOTION". The FDA issued a decision of Substantially Equivalent on May 21, 1986. The device falls under product code FZZ (Marker, Skin), a Class I device regulated under 21 CFR 878.4660.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 21, 1986
- Date Received
- May 7, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Marker, Skin
- Device Class
- Class I
- Regulation Number
- 878.4660
- Review Panel
- SU
- Submission Type