PORTADIAL CARRY-ON KIDNEY MACHINE
K-Number: K802297 · 1981-05-01
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Device Summary
Frequently Asked Questions
What is the PORTADIAL CARRY-ON KIDNEY MACHINE?
PORTADIAL CARRY-ON KIDNEY MACHINE is a medical device that received FDA 510(k) clearance on 1981-05-01. The listed applicant is Alan P. Kendal, Ph.D.. The 510(k) number is K802297.
When did PORTADIAL CARRY-ON KIDNEY MACHINE receive FDA 510(k) clearance?
PORTADIAL CARRY-ON KIDNEY MACHINE received FDA 510(k) clearance on 1981-05-01, under 510(k) number K802297.
Who is the listed applicant for PORTADIAL CARRY-ON KIDNEY MACHINE?
The FDA 510(k) record lists Alan P. Kendal, Ph.D. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PORTADIAL CARRY-ON KIDNEY MACHINE?
The FDA product code for PORTADIAL CARRY-ON KIDNEY MACHINE 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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