ClearanceBrief
Company ยท IL

Hospitech Respiration , Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 2010 to 2022. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
BSKCuff, Tracheal Tube, Inflatable4
BTPDropper, Ether1
JCXApparatus, Suction, Ward Use, Portable, Ac-Powered1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 29, 2022K221477AG100s
Hospitech Respiration , Ltd., IL
BSK
Oct 12, 2018K180991AG 100s
Hospitech Respiration , Ltd., IL
BSK
Feb 16, 2016K150157AnapnoGuard 100 Respiratory Guard System
Hospitech Respiration , Ltd., IL
BSK
May 13, 2013K131099AG MASS
Hospitech Respiration , Ltd., IL
JCX
May 3, 2013K122721AG GUFFILL
Hospitech Respiration , Ltd., IL
BSK
Mar 2, 2010K093126ANAPNOGUARD ENDOTRACHEAL TUBE
Hospitech Respiration , Ltd., IL
BTP

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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