510(k) K132614

PEREGRINE CURVED ILLUMINATING LASER PROBE by Peregrine Surgical , Ltd. — Product Code HQB

K132614 is an FDA 510(k) premarket notification submitted by Peregrine Surgical , Ltd. for the device "PEREGRINE CURVED ILLUMINATING LASER PROBE". The FDA issued a decision of Substantially Equivalent on November 14, 2013. The device falls under product code HQB (Photocoagulator And Accessories), a Class II device regulated under 21 CFR 886.4690. Peregrine Surgical , Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 14, 2013
Date Received
August 21, 2013
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Photocoagulator And Accessories
Device Class
Class II
Regulation Number
886.4690
Review Panel
OP
Submission Type