510(k) K843314
K843314 is an FDA 510(k) premarket notification submitted by Smith & Nephew, Mpl Division for the device "MPL HYPO BRAND BREECH LOAD ASPIR SYRINGE". The FDA issued a decision of Substantially Equivalent on September 27, 1984. The device falls under product code EJI (Syringe, Cartridge), a Class II device regulated under 21 CFR 872.6770. Smith & Nephew, Mpl Division has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 27, 1984
- Date Received
- August 24, 1984
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Syringe, Cartridge
- Device Class
- Class II
- Regulation Number
- 872.6770
- Review Panel
- DE
- Submission Type