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FDA 510(k)

NT MEDITENS PLUS, TYPE 290

K-Number: K014020 · 2002-07-11

ApplicantBio-Medical Research, Ltd.
Decision Date2002-07-11
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NT MEDITENS PLUS, TYPE 290 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 K014020. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NT MEDITENS PLUS, TYPE 290?

NT MEDITENS PLUS, TYPE 290 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 K014020.

When did NT MEDITENS PLUS, TYPE 290 receive FDA 510(k) clearance?

NT MEDITENS PLUS, TYPE 290 received FDA 510(k) clearance on 2002-07-11, under 510(k) number K014020.

Who is the listed applicant for NT MEDITENS PLUS, TYPE 290?

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 NT MEDITENS PLUS, TYPE 290?

The FDA product code for NT MEDITENS PLUS, TYPE 290 is GZJ.

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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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