Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SANODENT DOUBLE-ENDED INTERDENTAL CLEAN

K-Number: K832949 · 1983-10-04

Decision Date1983-10-04
Product CodeJET
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SANODENT DOUBLE-ENDED INTERDENTAL CLEAN is the device name listed in this FDA 510(k) record. The listed applicant is Coopercare, Inc.. It received FDA 510(k) clearance on 1983-10-04 under 510(k) number K832949. The device is classified under product code JET. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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.

↑