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FDA 510(k)

XRAY VISION

K-Number: K983111 · 1998-11-16

ApplicantApteryx, Inc.
Decision Date1998-11-16
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

XRAY VISION is the device name listed in this FDA 510(k) record. The listed applicant is Apteryx, Inc.. It received FDA 510(k) clearance on 1998-11-16 under 510(k) number K983111. 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 XRAY VISION?

XRAY VISION is a medical device that received FDA 510(k) clearance on 1998-11-16. The listed applicant is Apteryx, Inc.. The 510(k) number is K983111.

When did XRAY VISION receive FDA 510(k) clearance?

XRAY VISION received FDA 510(k) clearance on 1998-11-16, under 510(k) number K983111.

Who is the listed applicant for XRAY VISION?

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

What is the FDA product code for XRAY VISION?

The FDA product code for XRAY VISION is LLZ.

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Other records listing Apteryx, Inc. 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.

K182815XVWeb 3DK132342XVWEB

Related Devices (Code: LLZ)

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

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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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