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FDA 510(k)

FUNHALER, MODEL V-201E

K-Number: K072822 · 2007-11-26

ApplicantInfamed , Ltd.
Decision Date2007-11-26
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FUNHALER, MODEL V-201E is the device name listed in this FDA 510(k) record. The listed applicant is Infamed , Ltd.. It received FDA 510(k) clearance on 2007-11-26 under 510(k) number K072822. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FUNHALER, MODEL V-201E?

FUNHALER, MODEL V-201E is a medical device that received FDA 510(k) clearance on 2007-11-26. The listed applicant is Infamed , Ltd.. The 510(k) number is K072822.

When did FUNHALER, MODEL V-201E receive FDA 510(k) clearance?

FUNHALER, MODEL V-201E received FDA 510(k) clearance on 2007-11-26, under 510(k) number K072822.

Who is the listed applicant for FUNHALER, MODEL V-201E?

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

What is the FDA product code for FUNHALER, MODEL V-201E?

The FDA product code for FUNHALER, MODEL V-201E is CAF.

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Other records listing Infamed , 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.

K042546FUNHALER, MODEL FH 101

Related Devices (Code: CAF)

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

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