510(k) K843314

MPL HYPO BRAND BREECH LOAD ASPIR SYRINGE by Smith & Nephew, Mpl Division — Product Code EJI

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