SANODENT DOUBLE-ENDED INTERDENTAL CLEAN
K-Number: K832949 · 1983-10-04
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Device Summary
Frequently Asked Questions
What is the SANODENT DOUBLE-ENDED INTERDENTAL CLEAN?
SANODENT DOUBLE-ENDED INTERDENTAL CLEAN is a medical device that received FDA 510(k) clearance on 1983-10-04. The listed applicant is Coopercare, Inc.. The 510(k) number is K832949.
When did SANODENT DOUBLE-ENDED INTERDENTAL CLEAN receive FDA 510(k) clearance?
SANODENT DOUBLE-ENDED INTERDENTAL CLEAN received FDA 510(k) clearance on 1983-10-04, under 510(k) number K832949.
Who is the listed applicant for SANODENT DOUBLE-ENDED INTERDENTAL CLEAN?
The FDA 510(k) record lists Coopercare, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SANODENT DOUBLE-ENDED INTERDENTAL CLEAN?
The FDA product code for SANODENT DOUBLE-ENDED INTERDENTAL CLEAN is JET.
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 Coopercare, Inc. 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: JET)
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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