SALIVAN & SALIVAN BROWN
K-Number: K790097 · 1979-02-26
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Device Summary
Frequently Asked Questions
What is the SALIVAN & SALIVAN BROWN?
SALIVAN & SALIVAN BROWN is a medical device that received FDA 510(k) clearance on 1979-02-26. The listed applicant is Den-Mat Corp.. The 510(k) number is K790097.
When did SALIVAN & SALIVAN BROWN receive FDA 510(k) clearance?
SALIVAN & SALIVAN BROWN received FDA 510(k) clearance on 1979-02-26, under 510(k) number K790097.
Who is the listed applicant for SALIVAN & SALIVAN BROWN?
The FDA 510(k) record lists Den-Mat Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SALIVAN & SALIVAN BROWN?
The FDA product code for SALIVAN & SALIVAN BROWN is EJS.
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 Den-Mat 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: EJS)
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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