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FDA 510(k)

GUILD MAXOX GENERATOR (MAXOX)

K-Number: K901712 · 1991-02-27

ApplicantGuild Assoc., Inc.
Decision Date1991-02-27
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

GUILD MAXOX GENERATOR (MAXOX) is the device name listed in this FDA 510(k) record. The listed applicant is Guild Assoc., Inc.. It received FDA 510(k) clearance on 1991-02-27 under 510(k) number K901712. 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 GUILD MAXOX GENERATOR (MAXOX)?

GUILD MAXOX GENERATOR (MAXOX) is a medical device that received FDA 510(k) clearance on 1991-02-27. The listed applicant is Guild Assoc., Inc.. The 510(k) number is K901712.

When did GUILD MAXOX GENERATOR (MAXOX) receive FDA 510(k) clearance?

GUILD MAXOX GENERATOR (MAXOX) received FDA 510(k) clearance on 1991-02-27, under 510(k) number K901712.

Who is the listed applicant for GUILD MAXOX GENERATOR (MAXOX)?

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

What is the FDA product code for GUILD MAXOX GENERATOR (MAXOX)?

The FDA product code for GUILD MAXOX GENERATOR (MAXOX) is CAW.

Related Clinical Trials

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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Other records listing Guild Assoc., Inc. as applicant

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.

K903411FIELD MEDICAL OXYGEN GEN/DIST SYS-BATTLEFIELD PURP

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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