510(k) K123162
K123162 is an FDA 510(k) premarket notification submitted by U&U Medical Technology Co, Ltd. for the device "U&U HYDROGEN PEROXIDE GAS PLASMA STERILIZATION POUCH/ROLL". The FDA issued a decision of Substantially Equivalent on Feb 26, 2014. The device falls under product code FRG (Wrap, Sterilization), a Class II device regulated under 21 CFR 880.6850. U&U Medical Technology Co, Ltd. has 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 26, 2014
- Date Received
- Oct 9, 2012
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Wrap, Sterilization
- Device Class
- Class II
- Regulation Number
- 880.6850
- Review Panel
- HO
- Submission Type
- 510(k)