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FDA 510(k)

FLOSS N' GLOSS/SAFETY FLOSS MED DEVICE

K-Number: K841675 · 1984-06-27

ApplicantLeonard Lorch
Decision Date1984-06-27
Product CodeJES
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FLOSS N' GLOSS/SAFETY FLOSS MED DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Leonard Lorch. It received FDA 510(k) clearance on 1984-06-27 under 510(k) number K841675. 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 FLOSS N' GLOSS/SAFETY FLOSS MED DEVICE?

FLOSS N' GLOSS/SAFETY FLOSS MED DEVICE is a medical device that received FDA 510(k) clearance on 1984-06-27. The listed applicant is Leonard Lorch. The 510(k) number is K841675.

When did FLOSS N' GLOSS/SAFETY FLOSS MED DEVICE receive FDA 510(k) clearance?

FLOSS N' GLOSS/SAFETY FLOSS MED DEVICE received FDA 510(k) clearance on 1984-06-27, under 510(k) number K841675.

Who is the listed applicant for FLOSS N' GLOSS/SAFETY FLOSS MED DEVICE?

The FDA 510(k) record lists Leonard Lorch as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLOSS N' GLOSS/SAFETY FLOSS MED DEVICE?

The FDA product code for FLOSS N' GLOSS/SAFETY FLOSS MED DEVICE 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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