510(k) K152362
K152362 is an FDA 510(k) premarket notification submitted by Terumo (Philippines) Corporation for the device "Terumo SurGuard 3 Safety Hypodermic Needle". The FDA issued a decision of Substantially Equivalent on Oct 16, 2015. The device falls under product code FMI (Needle, Hypodermic, Single Lumen), a Class II device regulated under 21 CFR 880.5570. Terumo (Philippines) Corporation has 4 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 16, 2015
- Date Received
- Aug 20, 2015
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Needle, Hypodermic, Single Lumen
- Device Class
- Class II
- Regulation Number
- 880.5570
- Review Panel
- HO
- Submission Type
- 510(k)