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FDA 510(k)

MICROCAP PLUS/NPB-75

K-Number: K024300 · 2003-04-03

ApplicantOridion Medical 1987 , Ltd.
Decision Date2003-04-03
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICROCAP PLUS/NPB-75 is the device name listed in this FDA 510(k) record. The listed applicant is Oridion Medical 1987 , Ltd.. It received FDA 510(k) clearance on 2003-04-03 under 510(k) number K024300. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROCAP PLUS/NPB-75?

MICROCAP PLUS/NPB-75 is a medical device that received FDA 510(k) clearance on 2003-04-03. The listed applicant is Oridion Medical 1987 , Ltd.. The 510(k) number is K024300.

When did MICROCAP PLUS/NPB-75 receive FDA 510(k) clearance?

MICROCAP PLUS/NPB-75 received FDA 510(k) clearance on 2003-04-03, under 510(k) number K024300.

Who is the listed applicant for MICROCAP PLUS/NPB-75?

The FDA 510(k) record lists Oridion Medical 1987 , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROCAP PLUS/NPB-75?

The FDA product code for MICROCAP PLUS/NPB-75 is DQA.

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Related Devices (Code: DQA)

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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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