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

XPS STRAIGHTSHOT OR MODEL 2000 MICRODEBRIDER SYSTEM OR XPS POWERSCULPT

K Number: K992855 · Decision Jan 21, 2000
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
57
Applicant Total
82
Review Days
150

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Basic Information

Device Name
XPS STRAIGHTSHOT OR MODEL 2000 MICRODEBRIDER SYSTEM OR XPS POWERSCULPT
K Number
K992855
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5040
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Xomed, Inc.
Date Received
August 24, 1999
Decision Date
January 21, 2000
Product Code
QPB
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
QPB System, Suction, Lipoplasty For Removal

Similar 510(k) Clearances

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Other Clearances by Xomed, Inc.

K Number Device Name
K002395 MODEL 30 CLASSIC PNEUMATONOMETER
K002987 REDTRONIC XOMED MONOPOLAR ENERGIZED BLADE
K002828 XPS NITRO SYSTEM
K002897 TITANIUM MIDDLE EAR PROSTHESES
K993653 MICRO-FRANCE TROCARS AND ACCESSORIES
K001148 MEROGEL OTOLOGIC PACK
K994262 FRONTAL SINUS TREPHINATION CANNULA
K993582 MODIFICATION TO LASER-SHIELD II
K993655 MICRO-FRANCE ELECTROSURGICAL INSTRUMENTS, VARIOUS
K993112 XOMED ENT RF SYSTEM
Search all 82 clearances from Xomed, Inc. →