SCLERAL PLUGS, 19 AND 20 GAUGE
K-Number: K022186 · 2003-02-26
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Device Summary
Frequently Asked Questions
What is the SCLERAL PLUGS, 19 AND 20 GAUGE?
SCLERAL PLUGS, 19 AND 20 GAUGE is a medical device that received FDA 510(k) clearance on 2003-02-26. The listed applicant is Microvision, Inc.. The 510(k) number is K022186.
When did SCLERAL PLUGS, 19 AND 20 GAUGE receive FDA 510(k) clearance?
SCLERAL PLUGS, 19 AND 20 GAUGE received FDA 510(k) clearance on 2003-02-26, under 510(k) number K022186.
Who is the listed applicant for SCLERAL PLUGS, 19 AND 20 GAUGE?
The FDA 510(k) record lists Microvision, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SCLERAL PLUGS, 19 AND 20 GAUGE?
The FDA product code for SCLERAL PLUGS, 19 AND 20 GAUGE is LXP.
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 Microvision, 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: LXP)
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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