Hospitech Respiration , Ltd.

FDA Regulatory Profile

Hospitech Respiration , Ltd. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 29, 2022.

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K221477AG100sDecember 29, 2022
K180991AG 100sOctober 12, 2018
K150157AnapnoGuard 100 Respiratory Guard SystemFebruary 16, 2016
K131099AG MASSMay 13, 2013
K122721AG GUFFILLMay 3, 2013
K093126ANAPNOGUARD ENDOTRACHEAL TUBEMarch 2, 2010