EASYSTAT SODIUM/POTASSIUM ANALYZER
K-Number: K955375 · 1996-02-23
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Device Summary
Frequently Asked Questions
What is the EASYSTAT SODIUM/POTASSIUM ANALYZER?
EASYSTAT SODIUM/POTASSIUM ANALYZER is a medical device that received FDA 510(k) clearance on 1996-02-23. The listed applicant is Medica Corp.. The 510(k) number is K955375.
When did EASYSTAT SODIUM/POTASSIUM ANALYZER receive FDA 510(k) clearance?
EASYSTAT SODIUM/POTASSIUM ANALYZER received FDA 510(k) clearance on 1996-02-23, under 510(k) number K955375.
Who is the listed applicant for EASYSTAT SODIUM/POTASSIUM ANALYZER?
The FDA 510(k) record lists Medica Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EASYSTAT SODIUM/POTASSIUM ANALYZER?
The FDA product code for EASYSTAT SODIUM/POTASSIUM ANALYZER is JGS.
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 Medica Corp. 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: JGS)
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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