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FDA 510(k)

COMPUTER CONTROLLED EXTENSION (CCX)

K-Number: K863705 · 1987-01-06

ApplicantVarian Assoc., Inc.
Decision Date1987-01-06
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COMPUTER CONTROLLED EXTENSION (CCX) 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 1987-01-06 under 510(k) number K863705. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPUTER CONTROLLED EXTENSION (CCX)?

COMPUTER CONTROLLED EXTENSION (CCX) is a medical device that received FDA 510(k) clearance on 1987-01-06. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K863705.

When did COMPUTER CONTROLLED EXTENSION (CCX) receive FDA 510(k) clearance?

COMPUTER CONTROLLED EXTENSION (CCX) received FDA 510(k) clearance on 1987-01-06, under 510(k) number K863705.

Who is the listed applicant for COMPUTER CONTROLLED EXTENSION (CCX)?

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 COMPUTER CONTROLLED EXTENSION (CCX)?

The FDA product code for COMPUTER CONTROLLED EXTENSION (CCX) is IYE.

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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.

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Official Source

View on FDA Database →

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

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