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FDA 510(k)

RI MSC (MIGRATION SEDIMENTATION CHAMBER)

K-Number: K112413 · 2012-07-13

Decision Date2012-07-13
Product CodeMQK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

RI MSC (MIGRATION SEDIMENTATION CHAMBER) is the device name listed in this FDA 510(k) record. The listed applicant is Research Instruments , Ltd.. It received FDA 510(k) clearance on 2012-07-13 under 510(k) number K112413. The device is classified under product code MQK. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RI MSC (MIGRATION SEDIMENTATION CHAMBER)?

RI MSC (MIGRATION SEDIMENTATION CHAMBER) is a medical device that received FDA 510(k) clearance on 2012-07-13. The listed applicant is Research Instruments , Ltd.. The 510(k) number is K112413.

When did RI MSC (MIGRATION SEDIMENTATION CHAMBER) receive FDA 510(k) clearance?

RI MSC (MIGRATION SEDIMENTATION CHAMBER) received FDA 510(k) clearance on 2012-07-13, under 510(k) number K112413.

Who is the listed applicant for RI MSC (MIGRATION SEDIMENTATION CHAMBER)?

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

What is the FDA product code for RI MSC (MIGRATION SEDIMENTATION CHAMBER)?

The FDA product code for RI MSC (MIGRATION SEDIMENTATION CHAMBER) is MQK.

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.

Other records listing Research Instruments , Ltd. as applicant

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: MQK)

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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