BCM-ARC 105 X-RAY MOBILE UNIT
K-Number: K890306 · 1989-04-17
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Device Summary
Frequently Asked Questions
What is the BCM-ARC 105 X-RAY MOBILE UNIT?
BCM-ARC 105 X-RAY MOBILE UNIT is a medical device that received FDA 510(k) clearance on 1989-04-17. The listed applicant is B C Medical , Ltd.. The 510(k) number is K890306.
When did BCM-ARC 105 X-RAY MOBILE UNIT receive FDA 510(k) clearance?
BCM-ARC 105 X-RAY MOBILE UNIT received FDA 510(k) clearance on 1989-04-17, under 510(k) number K890306.
Who is the listed applicant for BCM-ARC 105 X-RAY MOBILE UNIT?
The FDA 510(k) record lists B C Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BCM-ARC 105 X-RAY MOBILE UNIT?
The FDA product code for BCM-ARC 105 X-RAY MOBILE 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 B C Medical , Ltd. 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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