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FDA 510(k)

MEDRELIEF SE SERIES, MODELS SE-50, SE-100, SE-200, SE-300

K-Number: K030998 · 2003-10-10

ApplicantHealthonics, Inc.
Decision Date2003-10-10
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MEDRELIEF SE SERIES, MODELS SE-50, SE-100, SE-200, SE-300 is the device name listed in this FDA 510(k) record. The listed applicant is Healthonics, Inc.. It received FDA 510(k) clearance on 2003-10-10 under 510(k) number K030998. 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 MEDRELIEF SE SERIES, MODELS SE-50, SE-100, SE-200, SE-300?

MEDRELIEF SE SERIES, MODELS SE-50, SE-100, SE-200, SE-300 is a medical device that received FDA 510(k) clearance on 2003-10-10. The listed applicant is Healthonics, Inc.. The 510(k) number is K030998.

When did MEDRELIEF SE SERIES, MODELS SE-50, SE-100, SE-200, SE-300 receive FDA 510(k) clearance?

MEDRELIEF SE SERIES, MODELS SE-50, SE-100, SE-200, SE-300 received FDA 510(k) clearance on 2003-10-10, under 510(k) number K030998.

Who is the listed applicant for MEDRELIEF SE SERIES, MODELS SE-50, SE-100, SE-200, SE-300?

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

What is the FDA product code for MEDRELIEF SE SERIES, MODELS SE-50, SE-100, SE-200, SE-300?

The FDA product code for MEDRELIEF SE SERIES, MODELS SE-50, SE-100, SE-200, SE-300 is IPF.

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 Healthonics, Inc. 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.

K060669MEDRELIEF ST SERIES, MODELS RT-50, ST-100, ST 150, ST-200, ST-300K003507MEDRELIEF

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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