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FDA 510(k)

EMPI CONTINUUM

K-Number: K093324 · 2010-03-05

ApplicantEmpi
Decision Date2010-03-05
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EMPI CONTINUUM is the device name listed in this FDA 510(k) record. The listed applicant is Empi. It received FDA 510(k) clearance on 2010-03-05 under 510(k) number K093324. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMPI CONTINUUM?

EMPI CONTINUUM is a medical device that received FDA 510(k) clearance on 2010-03-05. The listed applicant is Empi. The 510(k) number is K093324.

When did EMPI CONTINUUM receive FDA 510(k) clearance?

EMPI CONTINUUM received FDA 510(k) clearance on 2010-03-05, under 510(k) number K093324.

Who is the listed applicant for EMPI CONTINUUM?

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

What is the FDA product code for EMPI CONTINUUM?

The FDA product code for EMPI CONTINUUM is IPF.

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Other records listing Empi 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.

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Related Devices (Code: IPF)

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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