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FDA 510(k)

CATHETERIZATION TABLE KS-60

K-Number: K951315 · 1995-05-11

Decision Date1995-05-11
Product CodeIZZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CATHETERIZATION TABLE KS-60 is the device name listed in this FDA 510(k) record. The listed applicant is Shimadzu Medical Systems. It received FDA 510(k) clearance on 1995-05-11 under 510(k) number K951315. 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 CATHETERIZATION TABLE KS-60?

CATHETERIZATION TABLE KS-60 is a medical device that received FDA 510(k) clearance on 1995-05-11. The listed applicant is Shimadzu Medical Systems. The 510(k) number is K951315.

When did CATHETERIZATION TABLE KS-60 receive FDA 510(k) clearance?

CATHETERIZATION TABLE KS-60 received FDA 510(k) clearance on 1995-05-11, under 510(k) number K951315.

Who is the listed applicant for CATHETERIZATION TABLE KS-60?

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

What is the FDA product code for CATHETERIZATION TABLE KS-60?

The FDA product code for CATHETERIZATION TABLE KS-60 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 Shimadzu Medical Systems 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.

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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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