DRAGER MICRO VENT
K-Number: K953238 · 1996-09-16
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Device Summary
Frequently Asked Questions
What is the DRAGER MICRO VENT?
DRAGER MICRO VENT is a medical device that received FDA 510(k) clearance on 1996-09-16. The listed applicant is Drager, Inc.. The 510(k) number is K953238.
When did DRAGER MICRO VENT receive FDA 510(k) clearance?
DRAGER MICRO VENT received FDA 510(k) clearance on 1996-09-16, under 510(k) number K953238.
Who is the listed applicant for DRAGER MICRO VENT?
The FDA 510(k) record lists Drager, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DRAGER MICRO VENT?
The FDA product code for DRAGER MICRO VENT is CBK.
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 Drager, 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: CBK)
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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