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FDA 510(k)

BCM-ARC 105 X-RAY MOBILE UNIT

K-Number: K890306 · 1989-04-17

Decision Date1989-04-17
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BCM-ARC 105 X-RAY MOBILE UNIT is the device name listed in this FDA 510(k) record. The listed applicant is B C Medical , Ltd.. It received FDA 510(k) clearance on 1989-04-17 under 510(k) number K890306. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 8 devices →

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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