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Sechrist Industries, Inc.

SECHRIST INDUSTRIES, INC. · Model 3600HP-00-1 · UDI-DI 00852682007705

CBF Prescription

510(k) clearances

153

Adverse events (12 deaths)

Recalls

Facilities

Description

HBO CHMBR.ASSY.36IN,ENGLISH,BLUE,STORAGE

Recalls

Date	Firm	Reason
2014-08-08	Baro-Therapies, Inc	The firm is distributing the Rejuvenator device without an approved 510(k).
2008-08-28	Sechrist Industries Inc	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 perform
2008-08-28	Sechrist Industries Inc	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 perform

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.