510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K861360Substantially Equivalent

Maniquick Pedicure & Manicure Set

Quicklime Maniquick, Switzerland, CH / Traditional, Substantially Equivalent

K861360 is the FDA 510(k) clearance record for MANIQUICK PEDICURE & MANICURE SET, cleared for Quicklime Maniquick on . FDA records list one 510(k) clearance for Quicklime Maniquick. As of , FDA records show no recalls naming K861360.

Clearance record

Decision date
Received
(102 days to decision)
Review panel
Unknown
Applicant
Quicklime Maniquick 2738 Ct., Switzerland, CH
Third party review
No