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FDA 510(k)

MED-LOGICS MICROKERATOME BLADE, MODEL 7020CLB

K-Number: K022716 · 2002-10-11

Decision Date2002-10-11
Product CodeHNO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MED-LOGICS MICROKERATOME BLADE, MODEL 7020CLB is the device name listed in this FDA 510(k) record. The listed applicant is Med-Logics, Inc.. It received FDA 510(k) clearance on 2002-10-11 under 510(k) number K022716. The device is classified under product code HNO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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