MED-LOGICS MICROKERATOME BLADE, MODEL 7020CLB
K-Number: K022716 · 2002-10-11
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Device Summary
Frequently Asked Questions
What is the MED-LOGICS MICROKERATOME BLADE, MODEL 7020CLB?
MED-LOGICS MICROKERATOME BLADE, MODEL 7020CLB is a medical device that received FDA 510(k) clearance on 2002-10-11. The listed applicant is Med-Logics, Inc.. The 510(k) number is K022716.
When did MED-LOGICS MICROKERATOME BLADE, MODEL 7020CLB receive FDA 510(k) clearance?
MED-LOGICS MICROKERATOME BLADE, MODEL 7020CLB received FDA 510(k) clearance on 2002-10-11, under 510(k) number K022716.
Who is the listed applicant for MED-LOGICS MICROKERATOME BLADE, MODEL 7020CLB?
The FDA 510(k) record lists Med-Logics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MED-LOGICS MICROKERATOME BLADE, MODEL 7020CLB?
The FDA product code for MED-LOGICS MICROKERATOME BLADE, MODEL 7020CLB is HNO.
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 Med-Logics, 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: HNO)
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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