510(k) K151604

23ga Chandelier Illuminator, 25ga Chandelier Illuminator by Peregrine Surgical , Ltd. — Product Code MPA

K151604 is an FDA 510(k) premarket notification submitted by Peregrine Surgical , Ltd. for the device "23ga Chandelier Illuminator, 25ga Chandelier Illuminator". The FDA issued a decision of Substantially Equivalent on September 11, 2015. The device falls under product code MPA (Endoilluminator), a Class II device regulated under 21 CFR 876.1500. Peregrine Surgical , Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 11, 2015
Date Received
June 15, 2015
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Endoilluminator
Device Class
Class II
Regulation Number
876.1500
Review Panel
OP
Submission Type