510(k) K972883
K972883 is an FDA 510(k) premarket notification submitted by Cypress Medical Products, Ltd. for the device "ISOSAFE EARLOOP PROCEDURE MASK (BLUE, YELLOW)". The FDA issued a decision of Substantially Equivalent on February 26, 1998. The device falls under product code FXX (Mask, Surgical), a Class II device regulated under 21 CFR 878.4040. Cypress Medical Products, Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 26, 1998
- Date Received
- August 5, 1997
- 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