Sechrist Industries, Inc.CBFClass II

Chamber, Hyperbaric

Sechrist Industries, Inc.'s record for this product code

MDR events83All time

Recalls2All time

510(k) clearances5All time

Recent MDR events

83 adverse event reports on file

Recalls

2 recall events for this product code

TerminatedNov 6, 2012
Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with Electronic Control Modules in order to correct a software bug that could potentially affect the performance of the chamber.
View FDA record ↗
TerminatedNov 6, 2012
Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with Electronic Control Modules in order to correct a software bug that could potentially affect the performance of the chamber.
View FDA record ↗

510(k) clearances

5 clearances for this product code