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FDA 510(k)

HYDRA TRED DC

K-Number: K801250 · 1980-06-17

ApplicantMedichanics, Inc.
Decision Date1980-06-17
Product CodeIOG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HYDRA TRED DC is the device name listed in this FDA 510(k) record. The listed applicant is Medichanics, Inc.. It received FDA 510(k) clearance on 1980-06-17 under 510(k) number K801250. The device is classified under product code IOG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYDRA TRED DC?

HYDRA TRED DC is a medical device that received FDA 510(k) clearance on 1980-06-17. The listed applicant is Medichanics, Inc.. The 510(k) number is K801250.

When did HYDRA TRED DC receive FDA 510(k) clearance?

HYDRA TRED DC received FDA 510(k) clearance on 1980-06-17, under 510(k) number K801250.

Who is the listed applicant for HYDRA TRED DC?

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

What is the FDA product code for HYDRA TRED DC?

The FDA product code for HYDRA TRED DC is IOG.

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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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