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FDA 510(k)

NK MEDICAL MICROMETER, MODEL MC001

K-Number: K921266 · 1992-07-14

Decision Date1992-07-14
Product CodeKTZ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NK MEDICAL MICROMETER, MODEL MC001 is the device name listed in this FDA 510(k) record. The listed applicant is Nk Biotechnical Engineering Co.. It received FDA 510(k) clearance on 1992-07-14 under 510(k) number K921266. The device is classified under product code KTZ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NK MEDICAL MICROMETER, MODEL MC001?

NK MEDICAL MICROMETER, MODEL MC001 is a medical device that received FDA 510(k) clearance on 1992-07-14. The listed applicant is Nk Biotechnical Engineering Co.. The 510(k) number is K921266.

When did NK MEDICAL MICROMETER, MODEL MC001 receive FDA 510(k) clearance?

NK MEDICAL MICROMETER, MODEL MC001 received FDA 510(k) clearance on 1992-07-14, under 510(k) number K921266.

Who is the listed applicant for NK MEDICAL MICROMETER, MODEL MC001?

The FDA 510(k) record lists Nk Biotechnical Engineering Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NK MEDICAL MICROMETER, MODEL MC001?

The FDA product code for NK MEDICAL MICROMETER, MODEL MC001 is KTZ.

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 Nk Biotechnical Engineering Co. 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.

View all 15 devices →

Related Devices (Code: KTZ)

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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