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FDA 510(k)

X-SIGHT DIGITAL IMAGING SYSTEM

K-Number: K974134 · 1998-01-27

ApplicantStallion Technologies, Inc.
Decision Date1998-01-27
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

X-SIGHT DIGITAL IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stallion Technologies, Inc.. It received FDA 510(k) clearance on 1998-01-27 under 510(k) number K974134. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X-SIGHT DIGITAL IMAGING SYSTEM?

X-SIGHT DIGITAL IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 1998-01-27. The listed applicant is Stallion Technologies, Inc.. The 510(k) number is K974134.

When did X-SIGHT DIGITAL IMAGING SYSTEM receive FDA 510(k) clearance?

X-SIGHT DIGITAL IMAGING SYSTEM received FDA 510(k) clearance on 1998-01-27, under 510(k) number K974134.

Who is the listed applicant for X-SIGHT DIGITAL IMAGING SYSTEM?

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

What is the FDA product code for X-SIGHT DIGITAL IMAGING SYSTEM?

The FDA product code for X-SIGHT DIGITAL IMAGING SYSTEM is LLZ.

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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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