DIALYTE
K-Number: K823779 · 1983-01-17
Advertisement
Device Summary
Frequently Asked Questions
What is the DIALYTE?
DIALYTE is a medical device that received FDA 510(k) clearance on 1983-01-17. The listed applicant is Renal Dynamics, Inc.. The 510(k) number is K823779.
When did DIALYTE receive FDA 510(k) clearance?
DIALYTE received FDA 510(k) clearance on 1983-01-17, under 510(k) number K823779.
Who is the listed applicant for DIALYTE?
The FDA 510(k) record lists Renal Dynamics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIALYTE?
The FDA product code for DIALYTE 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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement