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FDA 510(k)

CHIN-UP STRIP

K-Number: K040491 · 2004-09-10

Decision Date2004-09-10
Product CodeLWF
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

CHIN-UP STRIP is the device name listed in this FDA 510(k) record. The listed applicant is Dale Miller, Inc. - the Chin-Up Company. It received FDA 510(k) clearance on 2004-09-10 under 510(k) number K040491. The device is classified under product code LWF. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHIN-UP STRIP?

CHIN-UP STRIP is a medical device that received FDA 510(k) clearance on 2004-09-10. The listed applicant is Dale Miller, Inc. - the Chin-Up Company. The 510(k) number is K040491.

When did CHIN-UP STRIP receive FDA 510(k) clearance?

CHIN-UP STRIP received FDA 510(k) clearance on 2004-09-10, under 510(k) number K040491.

Who is the listed applicant for CHIN-UP STRIP?

The FDA 510(k) record lists Dale Miller, Inc. - the Chin-Up Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHIN-UP STRIP?

The FDA product code for CHIN-UP STRIP is LWF.

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.

Related Devices (Code: LWF)

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.

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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