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FDA 510(k)

S500 SEATING SYSTEM

K-Number: K933863 · 1994-03-28

ApplicantFortress Scientific , Ltd.
Decision Date1994-03-28
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

S500 SEATING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Fortress Scientific , Ltd.. It received FDA 510(k) clearance on 1994-03-28 under 510(k) number K933863. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the S500 SEATING SYSTEM?

S500 SEATING SYSTEM is a medical device that received FDA 510(k) clearance on 1994-03-28. The listed applicant is Fortress Scientific , Ltd.. The 510(k) number is K933863.

When did S500 SEATING SYSTEM receive FDA 510(k) clearance?

S500 SEATING SYSTEM received FDA 510(k) clearance on 1994-03-28, under 510(k) number K933863.

Who is the listed applicant for S500 SEATING SYSTEM?

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

What is the FDA product code for S500 SEATING SYSTEM?

The FDA product code for S500 SEATING SYSTEM is ITI.

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Other records listing Fortress Scientific , Ltd. 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.

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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

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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