XTAL X-800 SHADOWGRAPH
K-Number: K861163 · 1986-05-06
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Device Summary
Frequently Asked Questions
What is the XTAL X-800 SHADOWGRAPH?
XTAL X-800 SHADOWGRAPH is a medical device that received FDA 510(k) clearance on 1986-05-06. The listed applicant is Xtal Corp.. The 510(k) number is K861163.
When did XTAL X-800 SHADOWGRAPH receive FDA 510(k) clearance?
XTAL X-800 SHADOWGRAPH received FDA 510(k) clearance on 1986-05-06, under 510(k) number K861163.
Who is the listed applicant for XTAL X-800 SHADOWGRAPH?
The FDA 510(k) record lists Xtal Corp. as the applicant. This does not by itself establish the device manufacturer.
Related Clinical Trials
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.
Other records listing Xtal Corp. 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.
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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