GERSON ISOLAIR APR PARTICULATE SURGICAL MASK
K-Number: K922507 · 1992-11-16
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Device Summary
Frequently Asked Questions
What is the GERSON ISOLAIR APR PARTICULATE SURGICAL MASK?
GERSON ISOLAIR APR PARTICULATE SURGICAL MASK is a medical device that received FDA 510(k) clearance on 1992-11-16. The listed applicant is Louis M. Gerson Co., Inc.. The 510(k) number is K922507.
When did GERSON ISOLAIR APR PARTICULATE SURGICAL MASK receive FDA 510(k) clearance?
GERSON ISOLAIR APR PARTICULATE SURGICAL MASK received FDA 510(k) clearance on 1992-11-16, under 510(k) number K922507.
Who is the listed applicant for GERSON ISOLAIR APR PARTICULATE SURGICAL MASK?
The FDA 510(k) record lists Louis M. Gerson Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GERSON ISOLAIR APR PARTICULATE SURGICAL MASK?
The FDA product code for GERSON ISOLAIR APR PARTICULATE SURGICAL MASK is FXX.
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 Louis M. Gerson Co., 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: FXX)
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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