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FDA 510(k)

UNIVERSAL VOL. VENTILATOR 72 #1626

K-Number: K832681 · 1983-09-26

Decision Date1983-09-26
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL VOL. VENTILATOR 72 #1626 is the device name listed in this FDA 510(k) record. The listed applicant is Hudson Oxygen Therapy Sales Co.. It received FDA 510(k) clearance on 1983-09-26 under 510(k) number K832681. The device is classified under product code BZO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIVERSAL VOL. VENTILATOR 72 #1626?

UNIVERSAL VOL. VENTILATOR 72 #1626 is a medical device that received FDA 510(k) clearance on 1983-09-26. The listed applicant is Hudson Oxygen Therapy Sales Co.. The 510(k) number is K832681.

When did UNIVERSAL VOL. VENTILATOR 72 #1626 receive FDA 510(k) clearance?

UNIVERSAL VOL. VENTILATOR 72 #1626 received FDA 510(k) clearance on 1983-09-26, under 510(k) number K832681.

Who is the listed applicant for UNIVERSAL VOL. VENTILATOR 72 #1626?

The FDA 510(k) record lists Hudson Oxygen Therapy Sales Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNIVERSAL VOL. VENTILATOR 72 #1626?

The FDA product code for UNIVERSAL VOL. VENTILATOR 72 #1626 is BZO.

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.

Other records listing Hudson Oxygen Therapy Sales Co. 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.

View all 33 devices →

Related Devices (Code: BZO)

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.

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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