FDA 510(k)

ALCYON ROTATIONAL COBALT THERAPY

K-Number: K837465 · 1983-06-28

Decision Date1983-06-28

Product Code

DecisionSubstantially Equivalent

Device Summary

ALCYON ROTATIONAL COBALT THERAPY 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 K837465. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALCYON ROTATIONAL COBALT THERAPY?

ALCYON ROTATIONAL COBALT THERAPY 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 K837465.

When did ALCYON ROTATIONAL COBALT THERAPY receive FDA 510(k) clearance?

ALCYON ROTATIONAL COBALT THERAPY received FDA 510(k) clearance on 1983-06-28, under 510(k) number K837465.

Who is the listed applicant for ALCYON ROTATIONAL COBALT THERAPY?

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

View on FDA Database →

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