510(k) K914960

INSTRUMENT ORGANIZER by O.R. Concepts, Inc. — Product Code KDC

K914960 is an FDA 510(k) premarket notification submitted by O.R. Concepts, Inc. for the device "INSTRUMENT ORGANIZER". The FDA issued a decision of Substantially Equivalent on February 28, 1992. The device falls under product code KDC (Instrument, Surgical, Disposable), a Class I device regulated under 21 CFR 878.4800. O.R. Concepts, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 28, 1992
Date Received
November 5, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Instrument, Surgical, Disposable
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type