FDA 510(k)

SATURNE I LINEAR ACCELERATOR

K-Number: K837412 · 1983-06-28

Decision Date1983-06-28

Product Code

DecisionSubstantially Equivalent

Device Summary

SATURNE I LINEAR ACCELERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Cgr Medical Corp.. It received FDA 510(k) clearance on 1983-06-28 under 510(k) number K837412. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SATURNE I LINEAR ACCELERATOR?

SATURNE I LINEAR ACCELERATOR is a medical device that received FDA 510(k) clearance on 1983-06-28. The listed applicant is Cgr Medical Corp.. The 510(k) number is K837412.

When did SATURNE I LINEAR ACCELERATOR receive FDA 510(k) clearance?

SATURNE I LINEAR ACCELERATOR received FDA 510(k) clearance on 1983-06-28, under 510(k) number K837412.

Who is the listed applicant for SATURNE I LINEAR ACCELERATOR?

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

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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.