HEMODIALYSIS CONCENTRATES AND RELATED PRODUCTS
K-Number: K860336 · 1986-03-04
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Device Summary
Frequently Asked Questions
What is the HEMODIALYSIS CONCENTRATES AND RELATED PRODUCTS?
HEMODIALYSIS CONCENTRATES AND RELATED PRODUCTS is a medical device that received FDA 510(k) clearance on 1986-03-04. The listed applicant is Breem Laboratories. The 510(k) number is K860336.
When did HEMODIALYSIS CONCENTRATES AND RELATED PRODUCTS receive FDA 510(k) clearance?
HEMODIALYSIS CONCENTRATES AND RELATED PRODUCTS received FDA 510(k) clearance on 1986-03-04, under 510(k) number K860336.
Who is the listed applicant for HEMODIALYSIS CONCENTRATES AND RELATED PRODUCTS?
The FDA 510(k) record lists Breem Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEMODIALYSIS CONCENTRATES AND RELATED PRODUCTS?
The FDA product code for HEMODIALYSIS CONCENTRATES AND RELATED PRODUCTS is FKQ.
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: FKQ)
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.
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