ClearanceBrief
Company ยท IT

Fiab Spa

FDA 510(k) clearances and medical device recalls filed under this name, 2009 to 2019. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FLLContinuous Measurement Thermometer3
GEIElectrosurgical, Cutting & Coagulation & Accessories1
GXYElectrode, Cutaneous1
HQPUnit, Cautery, Thermal, Battery-Powered1
LDDDc-Defibrillator, Low-Energy, (Including Paddles)1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 10, 2019K192210ESOTEST MULTI Esophageal Temperature Probe and Temperature Monitoring System
Fiab Spa, IT
FLL
Nov 8, 2018K180047ESOTEST MULTI Esophageal Temperature Probe and Temperature Monitoring System
Fiab Spa, IT
FLL
Feb 27, 2013K123361ESOTEST ESOPHAGEAL TEMPERATURE PROBE AND TEMPERATURE MONITORING SYSTEM
Fiab Spa, IT
FLL
Jun 16, 2011K103783EURO DEFI PADS ADULT; EURO DEFI PADS ADULT RADIOTRANSPARENT: EURO DEFI PADS PEDIATRIC
Fiab Spa, IT
LDD
Jun 21, 2010K100333FIAB SPA, MODELS F7244, F7233, F7234, F7277
Fiab Spa, IT
GEI
Sep 1, 2009K083428F7244, F7255, F7266, F7277, F7288, F7233, F7234 SERIES OF BATTERY-POWERED CAUTERY
Fiab Spa, IT
HQP
Jul 22, 2009K091163PG471W , PG471/50W, PG474W, PG477W, PG479/32W, PG479/50W, PG479/75W FIAB DISPOSABLE ELECTRODES WITH CABLE FOR ELECTRO-ST
Fiab Spa, IT
GXY

Latest recalls

DateFirm and productCodeLinked 510(k)
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