STANDARD S31
K-Number: K912307 · 1991-08-09
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Device Summary
Frequently Asked Questions
What is the STANDARD S31?
STANDARD S31 is a medical device that received FDA 510(k) clearance on 1991-08-09. The listed applicant is Metalor Dental USA Corp.. The 510(k) number is K912307.
When did STANDARD S31 receive FDA 510(k) clearance?
STANDARD S31 received FDA 510(k) clearance on 1991-08-09, under 510(k) number K912307.
Who is the listed applicant for STANDARD S31?
The FDA 510(k) record lists Metalor Dental USA Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STANDARD S31?
The FDA product code for STANDARD S31 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 Metalor Dental USA 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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