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FDA 510(k)

ACETATE-FREE DIALYSLATE SOLUTION

K-Number: K903835 · 1991-07-05

ApplicantPhysio, Inc.
Decision Date1991-07-05
Product CodeKPO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ACETATE-FREE DIALYSLATE SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Physio, Inc.. It received FDA 510(k) clearance on 1991-07-05 under 510(k) number K903835. The device is classified under product code KPO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACETATE-FREE DIALYSLATE SOLUTION?

ACETATE-FREE DIALYSLATE SOLUTION is a medical device that received FDA 510(k) clearance on 1991-07-05. The listed applicant is Physio, Inc.. The 510(k) number is K903835.

When did ACETATE-FREE DIALYSLATE SOLUTION receive FDA 510(k) clearance?

ACETATE-FREE DIALYSLATE SOLUTION received FDA 510(k) clearance on 1991-07-05, under 510(k) number K903835.

Who is the listed applicant for ACETATE-FREE DIALYSLATE SOLUTION?

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

What is the FDA product code for ACETATE-FREE DIALYSLATE SOLUTION?

The FDA product code for ACETATE-FREE DIALYSLATE SOLUTION is KPO.

Related Clinical Trials

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.

Related Devices (Code: KPO)

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.

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.

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