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FDA 510(k)

VARIAN/XIMATRON 5 CARBON-FIBER COUCH TOP

K-Number: K851653 · 1985-05-23

Decision Date1985-05-23
Product CodeKPQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VARIAN/XIMATRON 5 CARBON-FIBER COUCH TOP is the device name listed in this FDA 510(k) record. The listed applicant is Varian Assoc., Inc.. It received FDA 510(k) clearance on 1985-05-23 under 510(k) number K851653. The device is classified under product code KPQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VARIAN/XIMATRON 5 CARBON-FIBER COUCH TOP?

VARIAN/XIMATRON 5 CARBON-FIBER COUCH TOP is a medical device that received FDA 510(k) clearance on 1985-05-23. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K851653.

When did VARIAN/XIMATRON 5 CARBON-FIBER COUCH TOP receive FDA 510(k) clearance?

VARIAN/XIMATRON 5 CARBON-FIBER COUCH TOP received FDA 510(k) clearance on 1985-05-23, under 510(k) number K851653.

Who is the listed applicant for VARIAN/XIMATRON 5 CARBON-FIBER COUCH TOP?

The FDA 510(k) record lists Varian Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VARIAN/XIMATRON 5 CARBON-FIBER COUCH TOP?

The FDA product code for VARIAN/XIMATRON 5 CARBON-FIBER COUCH TOP is KPQ.

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 Varian Assoc., Inc. 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 86 devices →

Related Devices (Code: KPQ)

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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