ANALYZER, SODIUM/POTASSIUM NOVA L
K-Number: K770601 · 1977-06-14
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Device Summary
Frequently Asked Questions
What is the ANALYZER, SODIUM/POTASSIUM NOVA L?
ANALYZER, SODIUM/POTASSIUM NOVA L is a medical device that received FDA 510(k) clearance on 1977-06-14. The listed applicant is Nova Biomedical Corp.. The 510(k) number is K770601.
When did ANALYZER, SODIUM/POTASSIUM NOVA L receive FDA 510(k) clearance?
ANALYZER, SODIUM/POTASSIUM NOVA L received FDA 510(k) clearance on 1977-06-14, under 510(k) number K770601.
Who is the listed applicant for ANALYZER, SODIUM/POTASSIUM NOVA L?
The FDA 510(k) record lists Nova Biomedical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANALYZER, SODIUM/POTASSIUM NOVA L?
The FDA product code for ANALYZER, SODIUM/POTASSIUM NOVA L 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 Nova Biomedical 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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