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FDA 510(k)

LABORPRO SYSTEM

K-Number: K081984 · 2009-03-04

ApplicantTrig Medical, Ltd.
Decision Date2009-03-04
Product CodeNPB
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LABORPRO SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Trig Medical, Ltd.. It received FDA 510(k) clearance on 2009-03-04 under 510(k) number K081984. The device is classified under product code NPB. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LABORPRO SYSTEM?

LABORPRO SYSTEM is a medical device that received FDA 510(k) clearance on 2009-03-04. The listed applicant is Trig Medical, Ltd.. The 510(k) number is K081984.

When did LABORPRO SYSTEM receive FDA 510(k) clearance?

LABORPRO SYSTEM received FDA 510(k) clearance on 2009-03-04, under 510(k) number K081984.

Who is the listed applicant for LABORPRO SYSTEM?

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

What is the FDA product code for LABORPRO SYSTEM?

The FDA product code for LABORPRO SYSTEM is NPB.

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Related Devices (Code: NPB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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