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

ORIGIN SECONDARY CANNULA AND TROCAR

K Number: K922460 · Decision Sep 16, 1992
Classifications
1
FEI Numbers
378
Registration Numbers
378
Same Product Code
35
Applicant Total
50
Review Days
113

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Basic Information

Device Name
ORIGIN SECONDARY CANNULA AND TROCAR
K Number
K922460
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Origin Medsystems, Inc.
Date Received
May 26, 1992
Decision Date
September 16, 1992
Product Code
GEA
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
GEA Cannula, Surgical, General & Plastic Surgery

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K970611 ORIGIN CARDIAC STABLIZER OCCLUDER
K965121 CANNULA
K964171 VASOVIEW BALLOON DISSECTION SYSTEM
K962104 AIRLIFT BALLOON RETRACTON SYSTEM
K962005 EXTRAHAND BALLOON RETRACTOR
K960936 RESPOSABLE TROCAR SYSTEM [5MM, 5MM SHORT, 10MM AND 12MM SIZES]
K960637 5MM ENDOSCOPE
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