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FDA 510(k)

VAPORIZER, ANESTHESIA, NON-HEATED

K-Number: K882500 · 1988-08-01

Decision Date1988-08-01
Product CodeCAD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VAPORIZER, ANESTHESIA, NON-HEATED is the device name listed in this FDA 510(k) record. The listed applicant is Anesthetic Vaporizer Services. It received FDA 510(k) clearance on 1988-08-01 under 510(k) number K882500. The device is classified under product code CAD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAPORIZER, ANESTHESIA, NON-HEATED?

VAPORIZER, ANESTHESIA, NON-HEATED is a medical device that received FDA 510(k) clearance on 1988-08-01. The listed applicant is Anesthetic Vaporizer Services. The 510(k) number is K882500.

When did VAPORIZER, ANESTHESIA, NON-HEATED receive FDA 510(k) clearance?

VAPORIZER, ANESTHESIA, NON-HEATED received FDA 510(k) clearance on 1988-08-01, under 510(k) number K882500.

Who is the listed applicant for VAPORIZER, ANESTHESIA, NON-HEATED?

The FDA 510(k) record lists Anesthetic Vaporizer Services as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VAPORIZER, ANESTHESIA, NON-HEATED?

The FDA product code for VAPORIZER, ANESTHESIA, NON-HEATED is CAD.

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.

Related Devices (Code: CAD)

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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