ULTRAMATE 990
K-Number: K781114 · 1978-08-14
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Device Summary
Frequently Asked Questions
What is the ULTRAMATE 990?
ULTRAMATE 990 is a medical device that received FDA 510(k) clearance on 1978-08-14. The listed applicant is Litton Dental Products. The 510(k) number is K781114.
When did ULTRAMATE 990 receive FDA 510(k) clearance?
ULTRAMATE 990 received FDA 510(k) clearance on 1978-08-14, under 510(k) number K781114.
Who is the listed applicant for ULTRAMATE 990?
The FDA 510(k) record lists Litton Dental Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ULTRAMATE 990?
The FDA product code for ULTRAMATE 990 is EIA.
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 Litton Dental Products 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: EIA)
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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