Puritan-Bennett Companion Emt Liquid Oxygen

No FDA recalls on record, checked 9 Oct 2026.

510(k) Number

K895387 ↗

FDA Product Code

BYJ

Device Class

Class II

Regulation

21 CFR Part 868.5655

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

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  Class II

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  FDA 510(k) K993220 Active Cleared 22 Oct 1999

• Puritan-Bennett Aeris 590 Oxygen Concentrator with Oci

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  FDA 510(k) K993088 Active Cleared 8 Oct 1999

• Companion 318 Nasal Cpap Diagnostics System

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  FDA 510(k) K910194 Active Cleared 13 May 1991

• Puritan-Bennett Companion 320 I/E

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  FDA 510(k) K934804 Active Cleared 27 Feb 1995

• 7200 Microprocess Vent Sys/Model 7202 Display Opt

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  FDA 510(k) K862604 Active Cleared 1 Aug 1986

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