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FDA 510(k)

BETA 90/50 MOBILE IMAGING TABLE

K-Number: K884531 · 1989-01-11

Decision Date1989-01-11
Product CodeIXR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BETA 90/50 MOBILE IMAGING TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Beta Medical Products Co.. It received FDA 510(k) clearance on 1989-01-11 under 510(k) number K884531. The device is classified under product code IXR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BETA 90/50 MOBILE IMAGING TABLE?

BETA 90/50 MOBILE IMAGING TABLE is a medical device that received FDA 510(k) clearance on 1989-01-11. The listed applicant is Beta Medical Products Co.. The 510(k) number is K884531.

When did BETA 90/50 MOBILE IMAGING TABLE receive FDA 510(k) clearance?

BETA 90/50 MOBILE IMAGING TABLE received FDA 510(k) clearance on 1989-01-11, under 510(k) number K884531.

Who is the listed applicant for BETA 90/50 MOBILE IMAGING TABLE?

The FDA 510(k) record lists Beta Medical Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BETA 90/50 MOBILE IMAGING TABLE?

The FDA product code for BETA 90/50 MOBILE IMAGING 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 Beta Medical Products Co. 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

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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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