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FDA 510(k)

FORTRESS C-500 MICROPROCESSOR CONTROLLER

K-Number: K930088 · 1994-03-28

Decision Date1994-03-28
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FORTRESS C-500 MICROPROCESSOR CONTROLLER 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 K930088. 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 FORTRESS C-500 MICROPROCESSOR CONTROLLER?

FORTRESS C-500 MICROPROCESSOR CONTROLLER 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 K930088.

When did FORTRESS C-500 MICROPROCESSOR CONTROLLER receive FDA 510(k) clearance?

FORTRESS C-500 MICROPROCESSOR CONTROLLER received FDA 510(k) clearance on 1994-03-28, under 510(k) number K930088.

Who is the listed applicant for FORTRESS C-500 MICROPROCESSOR CONTROLLER?

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 FORTRESS C-500 MICROPROCESSOR CONTROLLER?

The FDA product code for FORTRESS C-500 MICROPROCESSOR CONTROLLER is ITI.

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.

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.

View all 27 devices →

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.

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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