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FDA 510(k)

PALL FIELD MEDICAL OXYGEN GENERA. & DISTRI. SYSTEM

K-Number: K873526 · 1988-02-29

ApplicantPall Safety Atmospheres, Inc.
Decision Date1988-02-29
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PALL FIELD MEDICAL OXYGEN GENERA. & DISTRI. SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Pall Safety Atmospheres, Inc.. It received FDA 510(k) clearance on 1988-02-29 under 510(k) number K873526. 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 PALL FIELD MEDICAL OXYGEN GENERA. & DISTRI. SYSTEM?

PALL FIELD MEDICAL OXYGEN GENERA. & DISTRI. SYSTEM is a medical device that received FDA 510(k) clearance on 1988-02-29. The listed applicant is Pall Safety Atmospheres, Inc.. The 510(k) number is K873526.

When did PALL FIELD MEDICAL OXYGEN GENERA. & DISTRI. SYSTEM receive FDA 510(k) clearance?

PALL FIELD MEDICAL OXYGEN GENERA. & DISTRI. SYSTEM received FDA 510(k) clearance on 1988-02-29, under 510(k) number K873526.

Who is the listed applicant for PALL FIELD MEDICAL OXYGEN GENERA. & DISTRI. SYSTEM?

The FDA 510(k) record lists Pall Safety Atmospheres, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PALL FIELD MEDICAL OXYGEN GENERA. & DISTRI. SYSTEM?

The FDA product code for PALL FIELD MEDICAL OXYGEN GENERA. & DISTRI. SYSTEM 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

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

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