EXR
K-Number: K771556 · 1977-08-22
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Device Summary
Frequently Asked Questions
What is the EXR?
EXR is a medical device that received FDA 510(k) clearance on 1977-08-22. The listed applicant is Litton Dental Products. The 510(k) number is K771556.
When did EXR receive FDA 510(k) clearance?
EXR received FDA 510(k) clearance on 1977-08-22, under 510(k) number K771556.
Who is the listed applicant for EXR?
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 EXR?
The FDA product code for EXR is ELC.
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: ELC)
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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