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FDA 510(k)

A921 12 VOLT POWER SOCKET

K-Number: K933856 · 1994-03-28

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

Device Summary

A921 12 VOLT POWER SOCKET 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 K933856. 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 A921 12 VOLT POWER SOCKET?

A921 12 VOLT POWER SOCKET 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 K933856.

When did A921 12 VOLT POWER SOCKET receive FDA 510(k) clearance?

A921 12 VOLT POWER SOCKET received FDA 510(k) clearance on 1994-03-28, under 510(k) number K933856.

Who is the listed applicant for A921 12 VOLT POWER SOCKET?

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 A921 12 VOLT POWER SOCKET?

The FDA product code for A921 12 VOLT POWER SOCKET 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.

K933855S490 SEATING SYSTEMK933864720 POWER BASEK933860S480 SEATING SYSTEMK933858730 POWER BASEK932597FORTRESS C-300 MICROPROCESSOR CONTROLLERK933853A901 TILT IN SPACE

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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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