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FDA 510(k)

PURITAN-BENNETT AERIS 590 OXYGEN CONCENTRATOR WITH OCI

K-Number: K993088 · 1999-10-08

ApplicantPuritan Bennett Corp.
Decision Date1999-10-08
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PURITAN-BENNETT AERIS 590 OXYGEN CONCENTRATOR WITH OCI is the device name listed in this FDA 510(k) record. The listed applicant is Puritan Bennett Corp.. It received FDA 510(k) clearance on 1999-10-08 under 510(k) number K993088. The device is classified under product code CAW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PURITAN-BENNETT AERIS 590 OXYGEN CONCENTRATOR WITH OCI?

PURITAN-BENNETT AERIS 590 OXYGEN CONCENTRATOR WITH OCI is a medical device that received FDA 510(k) clearance on 1999-10-08. The listed applicant is Puritan Bennett Corp.. The 510(k) number is K993088.

When did PURITAN-BENNETT AERIS 590 OXYGEN CONCENTRATOR WITH OCI receive FDA 510(k) clearance?

PURITAN-BENNETT AERIS 590 OXYGEN CONCENTRATOR WITH OCI received FDA 510(k) clearance on 1999-10-08, under 510(k) number K993088.

Who is the listed applicant for PURITAN-BENNETT AERIS 590 OXYGEN CONCENTRATOR WITH OCI?

The FDA 510(k) record lists Puritan Bennett Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PURITAN-BENNETT AERIS 590 OXYGEN CONCENTRATOR WITH OCI?

The FDA product code for PURITAN-BENNETT AERIS 590 OXYGEN CONCENTRATOR WITH OCI is CAW.

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Related Devices (Code: CAW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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