510(k) K833124

HOBBS MEDICAL RETRIEVAL BASKET by Hobbs Medical, Inc. — Product Code OCZ

K833124 is an FDA 510(k) premarket notification submitted by Hobbs Medical, Inc. for the device "HOBBS MEDICAL RETRIEVAL BASKET". The FDA issued a decision of Substantially Equivalent on November 29, 1983. The device falls under product code OCZ (Endoscopic Grasping/Cutting Instrument, Non-Powered), a Class II device regulated under 21 CFR 876.1500. Hobbs Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 29, 1983
Date Received
September 13, 1983
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.