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FDA 510(k)

BASS ANTALGIC-TRAK

K-Number: K042482 · 2005-03-21

Decision Date2005-03-21
Product CodeITH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BASS ANTALGIC-TRAK is the device name listed in this FDA 510(k) record. The listed applicant is Traction Masters, LLC. It received FDA 510(k) clearance on 2005-03-21 under 510(k) number K042482. The device is classified under product code ITH. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BASS ANTALGIC-TRAK?

BASS ANTALGIC-TRAK is a medical device that received FDA 510(k) clearance on 2005-03-21. The listed applicant is Traction Masters, LLC. The 510(k) number is K042482.

When did BASS ANTALGIC-TRAK receive FDA 510(k) clearance?

BASS ANTALGIC-TRAK received FDA 510(k) clearance on 2005-03-21, under 510(k) number K042482.

Who is the listed applicant for BASS ANTALGIC-TRAK?

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

What is the FDA product code for BASS ANTALGIC-TRAK?

The FDA product code for BASS ANTALGIC-TRAK is ITH.

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: ITH)

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

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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