FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇰 Denmark

SafeAir combi (SFR-combi-US)

K Number: K223932 · Decision Apr 26, 2023
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
16
Review Days
117

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
SafeAir combi (SFR-combi-US)
K Number
K223932
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
Lina Medical Aps
Date Received
December 30, 2022
Decision Date
April 26, 2023
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

Similar 510(k) Clearances

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

View all

Other Clearances by Lina Medical Aps

K Number Device Name
K240227 LiNA CystoVu™ HD (CYV-100-5; CYV-101-5); LiNA ScopeVu™ (SCP-100-1)
K221085 LiNA OperaScope Needle
K193007 LiNA OperaScope with HDMI cable and on-board LCD - 6 units, LiNA OperaScope Recording Module
K182224 SafeAir Smoke Evacuator compact
K182354 SafeAir Telescopic Smoke Pencil
K171113 LiNA OperaScope with HDMI cable and on-board LCD-single unit, LiNA OperaScope with HDMI cable and on-board LCD-6 units, LiNA OperaScope Recording Module
K143145 SafeAir Smoke Pencil
K142757 LiNA PowerBlade Plus HC
K142538 LiNA SafeAir Smoke Pencil
K132135 LINA GOLD LOOP HC
Search all 16 clearances from Lina Medical Aps →