D-VAPOR
K-Number: K042276 · 2004-09-23
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Device Summary
Frequently Asked Questions
What is the D-VAPOR?
D-VAPOR is a medical device that received FDA 510(k) clearance on 2004-09-23. The listed applicant is Draeger Medical, Inc.. The 510(k) number is K042276.
When did D-VAPOR receive FDA 510(k) clearance?
D-VAPOR received FDA 510(k) clearance on 2004-09-23, under 510(k) number K042276.
Who is the listed applicant for D-VAPOR?
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 D-VAPOR?
The FDA product code for D-VAPOR 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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