SALIVAN PARAEIGHT TOUGHNESS
K-Number: K790096 · 1979-02-26
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Device Summary
Frequently Asked Questions
What is the SALIVAN PARAEIGHT TOUGHNESS?
SALIVAN PARAEIGHT TOUGHNESS 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 K790096.
When did SALIVAN PARAEIGHT TOUGHNESS receive FDA 510(k) clearance?
SALIVAN PARAEIGHT TOUGHNESS received FDA 510(k) clearance on 1979-02-26, under 510(k) number K790096.
Who is the listed applicant for SALIVAN PARAEIGHT TOUGHNESS?
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 PARAEIGHT TOUGHNESS?
The FDA product code for SALIVAN PARAEIGHT TOUGHNESS 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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