FLUROPERM 60-OK, PARAGON HDS-OK
K-Number: K000224 · 2000-04-17
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Device Summary
Frequently Asked Questions
What is the FLUROPERM 60-OK, PARAGON HDS-OK?
FLUROPERM 60-OK, PARAGON HDS-OK is a medical device that received FDA 510(k) clearance on 2000-04-17. The listed applicant is Paragon Vision Sciences. The 510(k) number is K000224.
When did FLUROPERM 60-OK, PARAGON HDS-OK receive FDA 510(k) clearance?
FLUROPERM 60-OK, PARAGON HDS-OK received FDA 510(k) clearance on 2000-04-17, under 510(k) number K000224.
Who is the listed applicant for FLUROPERM 60-OK, PARAGON HDS-OK?
The FDA 510(k) record lists Paragon Vision Sciences as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLUROPERM 60-OK, PARAGON HDS-OK?
The FDA product code for FLUROPERM 60-OK, PARAGON HDS-OK is MUW.
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 Paragon Vision Sciences 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: MUW)
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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