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FDA 510(k)

BENNETT BCA-6 &BCA-9 MOBILE C-ARM UNIT/RADIO/FLOUR

K-Number: K883092 · 1988-10-13

Decision Date1988-10-13
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BENNETT BCA-6 &BCA-9 MOBILE C-ARM UNIT/RADIO/FLOUR is the device name listed in this FDA 510(k) record. The listed applicant is Bennett X-Ray Corp.. It received FDA 510(k) clearance on 1988-10-13 under 510(k) number K883092. 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 BENNETT BCA-6 &BCA-9 MOBILE C-ARM UNIT/RADIO/FLOUR?

BENNETT BCA-6 &BCA-9 MOBILE C-ARM UNIT/RADIO/FLOUR is a medical device that received FDA 510(k) clearance on 1988-10-13. The listed applicant is Bennett X-Ray Corp.. The 510(k) number is K883092.

When did BENNETT BCA-6 &BCA-9 MOBILE C-ARM UNIT/RADIO/FLOUR receive FDA 510(k) clearance?

BENNETT BCA-6 &BCA-9 MOBILE C-ARM UNIT/RADIO/FLOUR received FDA 510(k) clearance on 1988-10-13, under 510(k) number K883092.

Who is the listed applicant for BENNETT BCA-6 &BCA-9 MOBILE C-ARM UNIT/RADIO/FLOUR?

The FDA 510(k) record lists Bennett X-Ray Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BENNETT BCA-6 &BCA-9 MOBILE C-ARM UNIT/RADIO/FLOUR?

The FDA product code for BENNETT BCA-6 &BCA-9 MOBILE C-ARM UNIT/RADIO/FLOUR 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 Bennett X-Ray 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.

View all 23 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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