ANALYZER: NOVA 10 CRT ANALYZER & QUALI CONT MATER
K-Number: K923806 · 1992-09-29
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Device Summary
Frequently Asked Questions
What is the ANALYZER: NOVA 10 CRT ANALYZER & QUALI CONT MATER?
ANALYZER: NOVA 10 CRT ANALYZER & QUALI CONT MATER is a medical device that received FDA 510(k) clearance on 1992-09-29. The listed applicant is Nova Biomedical Corp.. The 510(k) number is K923806.
When did ANALYZER: NOVA 10 CRT ANALYZER & QUALI CONT MATER receive FDA 510(k) clearance?
ANALYZER: NOVA 10 CRT ANALYZER & QUALI CONT MATER received FDA 510(k) clearance on 1992-09-29, under 510(k) number K923806.
Who is the listed applicant for ANALYZER: NOVA 10 CRT ANALYZER & QUALI CONT MATER?
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: NOVA 10 CRT ANALYZER & QUALI CONT MATER?
The FDA product code for ANALYZER: NOVA 10 CRT ANALYZER & QUALI CONT MATER 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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