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FDA 510(k)

INTERFACE

K-Number: K092541 · 2010-11-09

ApplicantBiostructures
Decision Date2010-11-09
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INTERFACE is the device name listed in this FDA 510(k) record. The listed applicant is Biostructures. It received FDA 510(k) clearance on 2010-11-09 under 510(k) number K092541. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERFACE?

INTERFACE is a medical device that received FDA 510(k) clearance on 2010-11-09. The listed applicant is Biostructures. The 510(k) number is K092541.

When did INTERFACE receive FDA 510(k) clearance?

INTERFACE received FDA 510(k) clearance on 2010-11-09, under 510(k) number K092541.

Who is the listed applicant for INTERFACE?

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

What is the FDA product code for INTERFACE?

The FDA product code for INTERFACE is MQV.

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Related PubMed Literature

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.

PMID: 39420619Polymer-interface-tissue model to estimate leachable release from medical devices.Mathematical medicine and biology : a journal of the IMA ()PMID: 37288633[Roadmap of Medical Device for Implanted Brain-computer Interface].Zhongguo yi liao qi xie za zhi = Chinese journal of medical instrumentation ()PMID: 31162965Research: User Interface Software Errors in Medical Devices: Study of U.S. Recall Data.Biomedical instrumentation & technology ()

Related Devices (Code: MQV)

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Official Source

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