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FDA 510(k)

COLLIMASTER-90

K-Number: K911127 · 1991-09-19

ApplicantVarian Assoc., Inc.
Decision Date1991-09-19
Product CodeIZW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COLLIMASTER-90 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 1991-09-19 under 510(k) number K911127. The device is classified under product code IZW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLLIMASTER-90?

COLLIMASTER-90 is a medical device that received FDA 510(k) clearance on 1991-09-19. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K911127.

When did COLLIMASTER-90 receive FDA 510(k) clearance?

COLLIMASTER-90 received FDA 510(k) clearance on 1991-09-19, under 510(k) number K911127.

Who is the listed applicant for COLLIMASTER-90?

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 COLLIMASTER-90?

The FDA product code for COLLIMASTER-90 is IZW.

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Other records listing Varian Assoc., Inc. as applicant

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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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