'E-Z FLOSS' AND 'LAZY FLOSS'
K-Number: K860963 · 1986-03-26
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Device Summary
Frequently Asked Questions
What is the 'E-Z FLOSS' AND 'LAZY FLOSS'?
'E-Z FLOSS' AND 'LAZY FLOSS' is a medical device that received FDA 510(k) clearance on 1986-03-26. The listed applicant is Login Industries , Ltd.. The 510(k) number is K860963.
When did 'E-Z FLOSS' AND 'LAZY FLOSS' receive FDA 510(k) clearance?
'E-Z FLOSS' AND 'LAZY FLOSS' received FDA 510(k) clearance on 1986-03-26, under 510(k) number K860963.
Who is the listed applicant for 'E-Z FLOSS' AND 'LAZY FLOSS'?
The FDA 510(k) record lists Login Industries , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 'E-Z FLOSS' AND 'LAZY FLOSS'?
The FDA product code for 'E-Z FLOSS' AND 'LAZY 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.
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