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FDA 510(k)

MIGHTY MAN (DYNAMIC LINKERS)

K-Number: K993737 · 2000-03-20

ApplicantMedtech Products , Ltd.
Decision Date2000-03-20
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MIGHTY MAN (DYNAMIC LINKERS) is the device name listed in this FDA 510(k) record. The listed applicant is Medtech Products , Ltd.. It received FDA 510(k) clearance on 2000-03-20 under 510(k) number K993737. The device is classified under product code HIS. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIGHTY MAN (DYNAMIC LINKERS)?

MIGHTY MAN (DYNAMIC LINKERS) is a medical device that received FDA 510(k) clearance on 2000-03-20. The listed applicant is Medtech Products , Ltd.. The 510(k) number is K993737.

When did MIGHTY MAN (DYNAMIC LINKERS) receive FDA 510(k) clearance?

MIGHTY MAN (DYNAMIC LINKERS) received FDA 510(k) clearance on 2000-03-20, under 510(k) number K993737.

Who is the listed applicant for MIGHTY MAN (DYNAMIC LINKERS)?

The FDA 510(k) record lists Medtech Products , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MIGHTY MAN (DYNAMIC LINKERS)?

The FDA product code for MIGHTY MAN (DYNAMIC LINKERS) is HIS.

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Other records listing Medtech Products , Ltd. as applicant

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Related Devices (Code: HIS)

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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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