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FDA 510(k)

VENOMETER

K-Number: K983900 · 1999-01-29

ApplicantAdvanced Medical Technology , Ltd.
Decision Date1999-01-29
Product CodeJOM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VENOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Medical Technology , Ltd.. It received FDA 510(k) clearance on 1999-01-29 under 510(k) number K983900. The device is classified under product code JOM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENOMETER?

VENOMETER is a medical device that received FDA 510(k) clearance on 1999-01-29. The listed applicant is Advanced Medical Technology , Ltd.. The 510(k) number is K983900.

When did VENOMETER receive FDA 510(k) clearance?

VENOMETER received FDA 510(k) clearance on 1999-01-29, under 510(k) number K983900.

Who is the listed applicant for VENOMETER?

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

What is the FDA product code for VENOMETER?

The FDA product code for VENOMETER is JOM.

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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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