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FDA 510(k)

CLASSIC 4-WAY ELEVATING TABLE

K-Number: K912474 · 1991-09-16

Decision Date1991-09-16
Product CodeIZZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CLASSIC 4-WAY ELEVATING TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Continental X-Ray Corp.. It received FDA 510(k) clearance on 1991-09-16 under 510(k) number K912474. The device is classified under product code IZZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLASSIC 4-WAY ELEVATING TABLE?

CLASSIC 4-WAY ELEVATING TABLE is a medical device that received FDA 510(k) clearance on 1991-09-16. The listed applicant is Continental X-Ray Corp.. The 510(k) number is K912474.

When did CLASSIC 4-WAY ELEVATING TABLE receive FDA 510(k) clearance?

CLASSIC 4-WAY ELEVATING TABLE received FDA 510(k) clearance on 1991-09-16, under 510(k) number K912474.

Who is the listed applicant for CLASSIC 4-WAY ELEVATING TABLE?

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

What is the FDA product code for CLASSIC 4-WAY ELEVATING TABLE?

The FDA product code for CLASSIC 4-WAY ELEVATING TABLE is IZZ.

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 Continental 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 27 devices →

Related Devices (Code: IZZ)

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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