MOBILE X-RAY UNIT
K-Number: K894021 · 1989-09-01
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Device Summary
Frequently Asked Questions
What is the MOBILE X-RAY UNIT?
MOBILE X-RAY UNIT is a medical device that received FDA 510(k) clearance on 1989-09-01. The listed applicant is Ziehm International, Inc.. The 510(k) number is K894021.
When did MOBILE X-RAY UNIT receive FDA 510(k) clearance?
MOBILE X-RAY UNIT received FDA 510(k) clearance on 1989-09-01, under 510(k) number K894021.
Who is the listed applicant for MOBILE X-RAY UNIT?
The FDA 510(k) record lists Ziehm International, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOBILE X-RAY UNIT?
The FDA product code for MOBILE X-RAY UNIT is IZL.
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 Ziehm International, 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: IZL)
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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