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FDA 510(k)

APLAB, MODEL 801D0030

K-Number: K030379 · 2003-08-29

Decision Date2003-08-29
Product CodeMNR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

APLAB, MODEL 801D0030 is the device name listed in this FDA 510(k) record. The listed applicant is Sector Medical Corp.. It received FDA 510(k) clearance on 2003-08-29 under 510(k) number K030379. The device is classified under product code MNR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APLAB, MODEL 801D0030?

APLAB, MODEL 801D0030 is a medical device that received FDA 510(k) clearance on 2003-08-29. The listed applicant is Sector Medical Corp.. The 510(k) number is K030379.

When did APLAB, MODEL 801D0030 receive FDA 510(k) clearance?

APLAB, MODEL 801D0030 received FDA 510(k) clearance on 2003-08-29, under 510(k) number K030379.

Who is the listed applicant for APLAB, MODEL 801D0030?

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

What is the FDA product code for APLAB, MODEL 801D0030?

The FDA product code for APLAB, MODEL 801D0030 is MNR.

Related Clinical Trials

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.

Related Devices (Code: MNR)

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.

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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