CRYSTAL MASK
K-Number: K870206 · 1987-02-20
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Device Summary
Frequently Asked Questions
What is the CRYSTAL MASK?
CRYSTAL MASK is a medical device that received FDA 510(k) clearance on 1987-02-20. The listed applicant is Brunswick Mfg. Co., Inc.. The 510(k) number is K870206.
When did CRYSTAL MASK receive FDA 510(k) clearance?
CRYSTAL MASK received FDA 510(k) clearance on 1987-02-20, under 510(k) number K870206.
Who is the listed applicant for CRYSTAL MASK?
The FDA 510(k) record lists Brunswick Mfg. Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CRYSTAL MASK?
The FDA product code for CRYSTAL MASK is BYG.
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: BYG)
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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