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FDA 510(k)

ANESTHESIA GAS MACHINE

K-Number: K802116 · 1980-10-03

Decision Date1980-10-03
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANESTHESIA GAS MACHINE 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 1980-10-03 under 510(k) number K802116. The device is classified under product code BZC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANESTHESIA GAS MACHINE?

ANESTHESIA GAS MACHINE is a medical device that received FDA 510(k) clearance on 1980-10-03. The listed applicant is Puritan Bennett Corp.. The 510(k) number is K802116.

When did ANESTHESIA GAS MACHINE receive FDA 510(k) clearance?

ANESTHESIA GAS MACHINE received FDA 510(k) clearance on 1980-10-03, under 510(k) number K802116.

Who is the listed applicant for ANESTHESIA GAS MACHINE?

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 ANESTHESIA GAS MACHINE?

The FDA product code for ANESTHESIA GAS MACHINE is BZC.

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 Puritan Bennett Corp. 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 110 devices →

Related Devices (Code: BZC)

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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