FDA 510(k)

DIALYSIS CONCENTRATE

K-Number: K851319 · 1985-07-02

Decision Date1985-07-02

Product Code

DecisionSubstantially Equivalent

Device Summary

DIALYSIS CONCENTRATE is the device name listed in this FDA 510(k) record. The listed applicant is Ries Biologicals. It received FDA 510(k) clearance on 1985-07-02 under 510(k) number K851319. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIALYSIS CONCENTRATE?

DIALYSIS CONCENTRATE is a medical device that received FDA 510(k) clearance on 1985-07-02. The listed applicant is Ries Biologicals. The 510(k) number is K851319.

When did DIALYSIS CONCENTRATE receive FDA 510(k) clearance?

DIALYSIS CONCENTRATE received FDA 510(k) clearance on 1985-07-02, under 510(k) number K851319.

Who is the listed applicant for DIALYSIS CONCENTRATE?

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

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Other records listing Ries Biologicals as applicant

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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.