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

PELLEFIRM

K Number: K132949 · Decision Feb 20, 2014
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
77
Applicant Total
5
Review Days
154

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Basic Information

Device Name
PELLEFIRM
K Number
K132949
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ellman International, Inc.
Date Received
September 19, 2013
Decision Date
February 20, 2014
Product Code
PBX
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
PBX Massager, Vacuum, Radio Frequency Induced Heat

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (PBX), ordered by most recent decision date.

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Other Clearances by Ellman International, Inc.

K Number Device Name
K132665 PELLEVE GLIDESAFE 10MM, 15MM & 20MM HANDPIECE, PELLEVE S5 - IEC
K123366 SURGITRON 4.0 DUAL RF S5-IEC
K071343 ELLMAN NOBLE ALLOY ELECTRODES
K052241 DISC-FX SYSTEM