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FDA 510(k)

STEALTH PRODUCTS SEATING SYSTEM

K-Number: K050264 · 2005-02-11

ApplicantStealth Products
Decision Date2005-02-11
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STEALTH PRODUCTS SEATING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stealth Products. It received FDA 510(k) clearance on 2005-02-11 under 510(k) number K050264. 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 STEALTH PRODUCTS SEATING SYSTEM?

STEALTH PRODUCTS SEATING SYSTEM is a medical device that received FDA 510(k) clearance on 2005-02-11. The listed applicant is Stealth Products. The 510(k) number is K050264.

When did STEALTH PRODUCTS SEATING SYSTEM receive FDA 510(k) clearance?

STEALTH PRODUCTS SEATING SYSTEM received FDA 510(k) clearance on 2005-02-11, under 510(k) number K050264.

Who is the listed applicant for STEALTH PRODUCTS SEATING SYSTEM?

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

What is the FDA product code for STEALTH PRODUCTS SEATING SYSTEM?

The FDA product code for STEALTH PRODUCTS SEATING SYSTEM 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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