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FDA 510(k)

ASIMANAGER - AT

K-Number: K111356 · 2011-11-09

ApplicantArlington Scientific, Inc.
Decision Date2011-11-09
Product CodeJQT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ASIMANAGER - AT is the device name listed in this FDA 510(k) record. The listed applicant is Arlington Scientific, Inc.. It received FDA 510(k) clearance on 2011-11-09 under 510(k) number K111356. The device is classified under product code JQT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASIMANAGER - AT?

ASIMANAGER - AT is a medical device that received FDA 510(k) clearance on 2011-11-09. The listed applicant is Arlington Scientific, Inc.. The 510(k) number is K111356.

When did ASIMANAGER - AT receive FDA 510(k) clearance?

ASIMANAGER - AT received FDA 510(k) clearance on 2011-11-09, under 510(k) number K111356.

Who is the listed applicant for ASIMANAGER - AT?

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

What is the FDA product code for ASIMANAGER - AT?

The FDA product code for ASIMANAGER - AT is JQT.

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Related Devices (Code: JQT)

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.

K944185ISOSCANIsolab, Inc.K915332MODEL 795 FLUOROMETER/DENSITOMETERCiba Corning Diagnostics Corp.K885254TARGET READERV-Tech, Inc.K860645ELECTROPHORESIS DATA CENTER (EDC)Helena LaboratoriesK862956ICON READERHybritech, Inc.K853734APOLLO DENSITOMETERAstral Medical Systems

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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