510(k) K120084

ENDOSCOPIC RETRIEVAL DEVICE by United States Endoscopy Group, Inc. — Product Code OCZ

K120084 is an FDA 510(k) premarket notification submitted by United States Endoscopy Group, Inc. for the device "ENDOSCOPIC RETRIEVAL DEVICE". The FDA issued a decision of Substantially Equivalent on May 30, 2012. The device falls under product code OCZ (Endoscopic Grasping/Cutting Instrument, Non-Powered), a Class II device regulated under 21 CFR 876.1500. United States Endoscopy Group, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 30, 2012
Date Received
January 11, 2012
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Endoscopic Grasping/Cutting Instrument, Non-Powered
Device Class
Class II
Regulation Number
876.1500
Review Panel
GU
Submission Type

To manually grasp stones, tissues or other objects through an endoscope. To manipulate, sample or cut tissues through an endoscope.