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FDA 510(k)

MEDIPOINT

K-Number: K982961 · 1999-06-07

ApplicantMedipoint , Ltd.
Decision Date1999-06-07
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDIPOINT is the device name listed in this FDA 510(k) record. The listed applicant is Medipoint , Ltd.. It received FDA 510(k) clearance on 1999-06-07 under 510(k) number K982961. 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 MEDIPOINT?

MEDIPOINT is a medical device that received FDA 510(k) clearance on 1999-06-07. The listed applicant is Medipoint , Ltd.. The 510(k) number is K982961.

When did MEDIPOINT receive FDA 510(k) clearance?

MEDIPOINT received FDA 510(k) clearance on 1999-06-07, under 510(k) number K982961.

Who is the listed applicant for MEDIPOINT?

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

What is the FDA product code for MEDIPOINT?

The FDA product code for MEDIPOINT is GZJ.

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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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