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FDA 510(k)

FALCON DISK DRIVE SUBSYSTEM

K-Number: K902643 · 1990-07-09

ApplicantSokar, Inc.
Decision Date1990-07-09
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FALCON DISK DRIVE SUBSYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sokar, Inc.. It received FDA 510(k) clearance on 1990-07-09 under 510(k) number K902643. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FALCON DISK DRIVE SUBSYSTEM?

FALCON DISK DRIVE SUBSYSTEM is a medical device that received FDA 510(k) clearance on 1990-07-09. The listed applicant is Sokar, Inc.. The 510(k) number is K902643.

When did FALCON DISK DRIVE SUBSYSTEM receive FDA 510(k) clearance?

FALCON DISK DRIVE SUBSYSTEM received FDA 510(k) clearance on 1990-07-09, under 510(k) number K902643.

Who is the listed applicant for FALCON DISK DRIVE SUBSYSTEM?

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

What is the FDA product code for FALCON DISK DRIVE SUBSYSTEM?

The FDA product code for FALCON DISK DRIVE SUBSYSTEM is JAK.

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Related Devices (Code: JAK)

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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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