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FDA 510(k)

VITALSTIM EXPERIA

K-Number: K070425 · 2007-06-11

ApplicantChattanooga Group
Decision Date2007-06-11
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VITALSTIM EXPERIA is the device name listed in this FDA 510(k) record. The listed applicant is Chattanooga Group. It received FDA 510(k) clearance on 2007-06-11 under 510(k) number K070425. 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 VITALSTIM EXPERIA?

VITALSTIM EXPERIA is a medical device that received FDA 510(k) clearance on 2007-06-11. The listed applicant is Chattanooga Group. The 510(k) number is K070425.

When did VITALSTIM EXPERIA receive FDA 510(k) clearance?

VITALSTIM EXPERIA received FDA 510(k) clearance on 2007-06-11, under 510(k) number K070425.

Who is the listed applicant for VITALSTIM EXPERIA?

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

What is the FDA product code for VITALSTIM EXPERIA?

The FDA product code for VITALSTIM EXPERIA is IPF.

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Other records listing Chattanooga Group as applicant

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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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