IN VISION-PLUS NANO WITH NEUTRAL ADVANTAGE TECHNOLOGY
K-Number: K093489 · 2010-07-29
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Device Summary
Frequently Asked Questions
What is the IN VISION-PLUS NANO WITH NEUTRAL ADVANTAGE TECHNOLOGY?
IN VISION-PLUS NANO WITH NEUTRAL ADVANTAGE TECHNOLOGY is a medical device that received FDA 510(k) clearance on 2010-07-29. The listed applicant is Rymed Technologies, Inc.. The 510(k) number is K093489.
When did IN VISION-PLUS NANO WITH NEUTRAL ADVANTAGE TECHNOLOGY receive FDA 510(k) clearance?
IN VISION-PLUS NANO WITH NEUTRAL ADVANTAGE TECHNOLOGY received FDA 510(k) clearance on 2010-07-29, under 510(k) number K093489.
Who is the listed applicant for IN VISION-PLUS NANO WITH NEUTRAL ADVANTAGE TECHNOLOGY?
The FDA 510(k) record lists Rymed Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IN VISION-PLUS NANO WITH NEUTRAL ADVANTAGE TECHNOLOGY?
The FDA product code for IN VISION-PLUS NANO WITH NEUTRAL ADVANTAGE TECHNOLOGY is FPA.
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 Rymed Technologies, Inc. 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: FPA)
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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