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FDA 510(k)

CORRIDOR4DM V2010 MODEL: V2010

K-Number: K101279 · 2010-08-04

ApplicantInvia
Decision Date2010-08-04
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CORRIDOR4DM V2010 MODEL: V2010 is the device name listed in this FDA 510(k) record. The listed applicant is Invia. It received FDA 510(k) clearance on 2010-08-04 under 510(k) number K101279. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORRIDOR4DM V2010 MODEL: V2010?

CORRIDOR4DM V2010 MODEL: V2010 is a medical device that received FDA 510(k) clearance on 2010-08-04. The listed applicant is Invia. The 510(k) number is K101279.

When did CORRIDOR4DM V2010 MODEL: V2010 receive FDA 510(k) clearance?

CORRIDOR4DM V2010 MODEL: V2010 received FDA 510(k) clearance on 2010-08-04, under 510(k) number K101279.

Who is the listed applicant for CORRIDOR4DM V2010 MODEL: V2010?

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

What is the FDA product code for CORRIDOR4DM V2010 MODEL: V2010?

The FDA product code for CORRIDOR4DM V2010 MODEL: V2010 is LLZ.

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.

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Other records listing Invia 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.

K080575CORRIDOR4DM

Related Devices (Code: LLZ)

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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