DRAGER VAPOR 19.1 ANESTHETIC VAPORIZERS
K-Number: K821650 · 1982-06-29
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Device Summary
Frequently Asked Questions
What is the DRAGER VAPOR 19.1 ANESTHETIC VAPORIZERS?
DRAGER VAPOR 19.1 ANESTHETIC VAPORIZERS is a medical device that received FDA 510(k) clearance on 1982-06-29. The listed applicant is Draeger Medical, Inc.. The 510(k) number is K821650.
When did DRAGER VAPOR 19.1 ANESTHETIC VAPORIZERS receive FDA 510(k) clearance?
DRAGER VAPOR 19.1 ANESTHETIC VAPORIZERS received FDA 510(k) clearance on 1982-06-29, under 510(k) number K821650.
Who is the listed applicant for DRAGER VAPOR 19.1 ANESTHETIC VAPORIZERS?
The FDA 510(k) record lists Draeger Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DRAGER VAPOR 19.1 ANESTHETIC VAPORIZERS?
The FDA product code for DRAGER VAPOR 19.1 ANESTHETIC VAPORIZERS 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.
Other records listing Draeger Medical, 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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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