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FDA 510(k)

K-TECH 2 POWER TILT SEATING SYSTEM, MODEL K2PT

K-Number: K033263 · 2003-10-31

ApplicantTrack Corporation
Decision Date2003-10-31
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

K-TECH 2 POWER TILT SEATING SYSTEM, MODEL K2PT is the device name listed in this FDA 510(k) record. The listed applicant is Track Corporation. It received FDA 510(k) clearance on 2003-10-31 under 510(k) number K033263. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the K-TECH 2 POWER TILT SEATING SYSTEM, MODEL K2PT?

K-TECH 2 POWER TILT SEATING SYSTEM, MODEL K2PT is a medical device that received FDA 510(k) clearance on 2003-10-31. The listed applicant is Track Corporation. The 510(k) number is K033263.

When did K-TECH 2 POWER TILT SEATING SYSTEM, MODEL K2PT receive FDA 510(k) clearance?

K-TECH 2 POWER TILT SEATING SYSTEM, MODEL K2PT received FDA 510(k) clearance on 2003-10-31, under 510(k) number K033263.

Who is the listed applicant for K-TECH 2 POWER TILT SEATING SYSTEM, MODEL K2PT?

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

What is the FDA product code for K-TECH 2 POWER TILT SEATING SYSTEM, MODEL K2PT?

The FDA product code for K-TECH 2 POWER TILT SEATING SYSTEM, MODEL K2PT is ITI.

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Related Devices (Code: ITI)

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

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