TELESTATIX X-RAY TABLE
K-Number: K883162 · 1988-09-06
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Device Summary
Frequently Asked Questions
What is the TELESTATIX X-RAY TABLE?
TELESTATIX X-RAY TABLE is a medical device that received FDA 510(k) clearance on 1988-09-06. The listed applicant is Bay X-Ray, Inc.. The 510(k) number is K883162.
When did TELESTATIX X-RAY TABLE receive FDA 510(k) clearance?
TELESTATIX X-RAY TABLE received FDA 510(k) clearance on 1988-09-06, under 510(k) number K883162.
Who is the listed applicant for TELESTATIX X-RAY TABLE?
The FDA 510(k) record lists Bay X-Ray, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TELESTATIX X-RAY TABLE?
The FDA product code for TELESTATIX X-RAY TABLE is IXR.
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 Bay X-Ray, 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.
Related Devices (Code: IXR)
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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