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FDA 510(k)

NEUROTECH MEDISTIM PLUS, TYPE 291

K-Number: K014019 · 2002-07-11

ApplicantBio-Medical Research, Ltd.
Decision Date2002-07-11
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NEUROTECH MEDISTIM PLUS, TYPE 291 is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Medical Research, Ltd.. It received FDA 510(k) clearance on 2002-07-11 under 510(k) number K014019. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROTECH MEDISTIM PLUS, TYPE 291?

NEUROTECH MEDISTIM PLUS, TYPE 291 is a medical device that received FDA 510(k) clearance on 2002-07-11. The listed applicant is Bio-Medical Research, Ltd.. The 510(k) number is K014019.

When did NEUROTECH MEDISTIM PLUS, TYPE 291 receive FDA 510(k) clearance?

NEUROTECH MEDISTIM PLUS, TYPE 291 received FDA 510(k) clearance on 2002-07-11, under 510(k) number K014019.

Who is the listed applicant for NEUROTECH MEDISTIM PLUS, TYPE 291?

The FDA 510(k) record lists Bio-Medical Research, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEUROTECH MEDISTIM PLUS, TYPE 291?

The FDA product code for NEUROTECH MEDISTIM PLUS, TYPE 291 is IPF.

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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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