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

Ranfac Fat Aspiration Cannula

K Number: K162932 · Decision Jan 19, 2017
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
39
Applicant Total
12
Review Days
91

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Basic Information

Device Name
Ranfac Fat Aspiration Cannula
K Number
K162932
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
Ranfac, Corp.
Date Received
October 20, 2016
Decision Date
January 19, 2017
Product Code
MUU
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
MUU System, Suction, Lipoplasty

Similar 510(k) Clearances

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

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Other Clearances by Ranfac, Corp.

K Number Device Name
K150156 Ranfac Fat Aspiration Transfer Syringe (FATS) Procedure Pack, Ranfac Fat Aspiration Transfer Syringe (FATS) Containment Vessel
K150563 Marrow Cellution Bone Marrow Aspiration Needle
K140991 RANFAC ASPIRATION NEEDLE WITH ADJUSTABLE GUIDE
K131157 RANFAC BONE MARROW ASPIRATION NEEDLE
K031344 RANFAC GOLDENBERG SNARECOIL SOFT TISSUE BIOPSY (GSS) NEEDLE
K012224 SINGLE ACTION BIOPSY NEEDLE, MODEL RCBS: XX GAUGE, XX LENGTH, XX THROW
K961922 RDP-2
K951090 INTRODUCER
K930474 NEEDLE, PNEUMOPERITONEUM, SPRING LOADED
K864139 RANFAC CUT BIOPSY NEEDLE
Search all 12 clearances from Ranfac, Corp. →