510(k) K946219

POP-N-LOK SYRINGE by Retractable Technologies, Inc. — Product Code MEG

K946219 is an FDA 510(k) premarket notification submitted by Retractable Technologies, Inc. for the device "POP-N-LOK SYRINGE". The FDA issued a decision of Substantially Equivalent on December 28, 1995. The device falls under product code MEG (Syringe, Antistick), a Class II device regulated under 21 CFR 880.5860. Retractable Technologies, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 28, 1995
Date Received
December 21, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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