510(k) K133635

EASYPOINT NEEDLE by Retractable Technologies, Inc. — Product Code FMI

K133635 is an FDA 510(k) premarket notification submitted by Retractable Technologies, Inc. for the device "EASYPOINT NEEDLE". The FDA issued a decision of Substantially Equivalent on June 17, 2014. The device falls under product code FMI (Needle, Hypodermic, Single Lumen), a Class II device regulated under 21 CFR 880.5570. Retractable Technologies, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 17, 2014
Date Received
November 26, 2013
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