510(k) K201624

Spin Care Disposable Protective Mask by Spintech, LLC — Product Code FXX

K201624 is an FDA 510(k) premarket notification submitted by Spintech, LLC for the device "Spin Care Disposable Protective Mask". The FDA issued a decision of Substantially Equivalent on March 18, 2021. The device falls under product code FXX (Mask, Surgical), a Class II device regulated under 21 CFR 878.4040. Spintech, LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 18, 2021
Date Received
June 15, 2020
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mask, Surgical
Device Class
Class II
Regulation Number
878.4040
Review Panel
HO
Submission Type