TWILIGHT FULL FACE MASK
K-Number: K070321 · 2007-04-30
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Device Summary
Frequently Asked Questions
What is the TWILIGHT FULL FACE MASK?
TWILIGHT FULL FACE MASK is a medical device that received FDA 510(k) clearance on 2007-04-30. The listed applicant is Invacare Corp.. The 510(k) number is K070321.
When did TWILIGHT FULL FACE MASK receive FDA 510(k) clearance?
TWILIGHT FULL FACE MASK received FDA 510(k) clearance on 2007-04-30, under 510(k) number K070321.
Who is the listed applicant for TWILIGHT FULL FACE MASK?
The FDA 510(k) record lists Invacare Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TWILIGHT FULL FACE MASK?
The FDA product code for TWILIGHT FULL FACE MASK is BZD.
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 Invacare 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.
Related Devices (Code: BZD)
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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