510(k) K121607
K121607 is an FDA 510(k) premarket notification submitted by Terumo (Philippines) Corporation for the device "TERUMO(R) NEEDLE". The FDA issued a decision of Substantially Equivalent on Nov 8, 2012. 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
- Nov 8, 2012
- Date Received
- Jun 1, 2012
- Clearance Type
- Traditional
- 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)