FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DORNOCH DUO SUCTION CART WITH: DL2800 LID, CL500 LID, DORNOCH QUAD SUCTION CART WITH: DL2800 LID, CL500 LID

K Number: K133786 · Decision Mar 21, 2014
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
76
Applicant Total
3
Review Days
99

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Basic Information

Device Name
DORNOCH DUO SUCTION CART WITH: DL2800 LID, CL500 LID, DORNOCH QUAD SUCTION CART WITH: DL2800 LID, CL500 LID
K Number
K133786
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4780
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dornoch Medical Systems, Inc.
Date Received
December 12, 2013
Decision Date
March 21, 2014
Product Code
JCX
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
JCX Apparatus, Suction, Ward Use, Portable, Ac-Powered

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Other Clearances by Dornoch Medical Systems, Inc.

K Number Device Name
K123188 DORNOCH DUO SUCTION CART WITH DL2800 LID MODEL UL-DU2800, DORNOCH DUO SUCTION CART WITH CL500 LID MODEL UL-DU500, DORNOC
K081047 TRANSPOSAL ULTRA SYSTEMS