510(k) K864779

MACLEE/BOIN MEDICA STERILE NEEDLE/SYRINGE 50ML/CC by Mac Lee Medical Products — Product Code FMF

K864779 is an FDA 510(k) premarket notification submitted by Mac Lee Medical Products for the device "MACLEE/BOIN MEDICA STERILE NEEDLE/SYRINGE 50ML/CC". The FDA issued a decision of Substantially Equivalent on December 29, 1986. The device falls under product code FMF (Syringe, Piston), a Class II device regulated under 21 CFR 880.5860. Mac Lee Medical Products has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 29, 1986
Date Received
December 8, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Syringe, Piston
Device Class
Class II
Regulation Number
880.5860
Review Panel
HO
Submission Type