FLOSS N' GLOSS/SAFETY FLOSS MED DEVICE
K-Number: K841675 · 1984-06-27
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Device Summary
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
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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