FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

INSTRUMENT ORGANIZER

K Number: K914960 · Decision Feb 28, 1992
Classifications
1
FEI Numbers
231
Registration Numbers
231
Same Product Code
66
Applicant Total
34
Review Days
115

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Basic Information

Device Name
INSTRUMENT ORGANIZER
K Number
K914960
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
O.R. Concepts, Inc.
Date Received
November 5, 1991
Decision Date
February 28, 1992
Product Code
KDC
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KDC Instrument, Surgical, Disposable

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Other Clearances by O.R. Concepts, Inc.

K Number Device Name
K941337 FLOWGUN ELECTROCAUTERY PROBES
K935970 FLOWGUN ELECTROCAUTERY PROBE HANDLE
K935971 FLOWGUN ELECTROCAUTERY PROBES
K935645 FLOWGUN REUSABLE IRRIGATION PROBES
K926242 ORC ENDOSCOPIC MONOPOLAR ELECTROSURGICAL PROBE
K922244 INSUFFLATOR TUBING/FILTER KIT
K922197 INSUFFLATOR TUBING KIT
K932449 DR. FOG
K925147 ORC 10.0MM SUCTION PROBE
K925024 ORC TAPPERED IRRIGATING PROBE
Search all 34 clearances from O.R. Concepts, Inc. →