PHOENIX DIALYSATE METER
K-Number: K955298 · 1996-02-29
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Device Summary
Frequently Asked Questions
What is the PHOENIX DIALYSATE METER?
PHOENIX DIALYSATE METER is a medical device that received FDA 510(k) clearance on 1996-02-29. The listed applicant is Automata Medical Instrumentation, Inc.. The 510(k) number is K955298.
When did PHOENIX DIALYSATE METER receive FDA 510(k) clearance?
PHOENIX DIALYSATE METER received FDA 510(k) clearance on 1996-02-29, under 510(k) number K955298.
Who is the listed applicant for PHOENIX DIALYSATE METER?
The FDA 510(k) record lists Automata Medical Instrumentation, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PHOENIX DIALYSATE METER?
The FDA product code for PHOENIX DIALYSATE METER is FIZ.
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.
Other records listing Automata Medical Instrumentation, Inc. as applicant
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: FIZ)
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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