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FDA 510(k)

CSL X-RAY IMAGESCOPE

K-Number: K923137 · 1992-09-23

ApplicantCsi Opto-Electronics Corp.
Decision Date1992-09-23
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CSL X-RAY IMAGESCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Csi Opto-Electronics Corp.. It received FDA 510(k) clearance on 1992-09-23 under 510(k) number K923137. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CSL X-RAY IMAGESCOPE?

CSL X-RAY IMAGESCOPE is a medical device that received FDA 510(k) clearance on 1992-09-23. The listed applicant is Csi Opto-Electronics Corp.. The 510(k) number is K923137.

When did CSL X-RAY IMAGESCOPE receive FDA 510(k) clearance?

CSL X-RAY IMAGESCOPE received FDA 510(k) clearance on 1992-09-23, under 510(k) number K923137.

Who is the listed applicant for CSL X-RAY IMAGESCOPE?

The FDA 510(k) record lists Csi Opto-Electronics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CSL X-RAY IMAGESCOPE?

The FDA product code for CSL X-RAY IMAGESCOPE is JAA.

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Related Devices (Code: JAA)

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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