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)

GENTLE FLOSS

K-Number: K792493 · 1979-12-13

Decision Date1979-12-13
Product CodeJES
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GENTLE FLOSS is the device name listed in this FDA 510(k) record. The listed applicant is Paul E. Jaffe, D.M.D.. It received FDA 510(k) clearance on 1979-12-13 under 510(k) number K792493. The device is classified under product code JES. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENTLE FLOSS?

GENTLE FLOSS is a medical device that received FDA 510(k) clearance on 1979-12-13. The listed applicant is Paul E. Jaffe, D.M.D.. The 510(k) number is K792493.

When did GENTLE FLOSS receive FDA 510(k) clearance?

GENTLE FLOSS received FDA 510(k) clearance on 1979-12-13, under 510(k) number K792493.

Who is the listed applicant for GENTLE FLOSS?

The FDA 510(k) record lists Paul E. Jaffe, D.M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GENTLE FLOSS?

The FDA product code for GENTLE FLOSS is JES.

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.

Related Devices (Code: JES)

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.

↑