NOVA DIAMOND
K-Number: K885233 · 1989-02-13
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Device Summary
Frequently Asked Questions
What is the NOVA DIAMOND?
NOVA DIAMOND is a medical device that received FDA 510(k) clearance on 1989-02-13. The listed applicant is Microcopy, Div. Neo-Flo, Inc.. The 510(k) number is K885233.
When did NOVA DIAMOND receive FDA 510(k) clearance?
NOVA DIAMOND received FDA 510(k) clearance on 1989-02-13, under 510(k) number K885233.
Who is the listed applicant for NOVA DIAMOND?
The FDA 510(k) record lists Microcopy, Div. Neo-Flo, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NOVA DIAMOND?
The FDA product code for NOVA DIAMOND is DZP.
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 Microcopy, Div. Neo-Flo, 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: DZP)
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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