SUN FLOWER SOLETTE MINETTE NOVA SUPER 28X, PRO SER
K-Number: K851408 · 1985-07-05
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Device Summary
Frequently Asked Questions
What is the SUN FLOWER SOLETTE MINETTE NOVA SUPER 28X, PRO SER?
SUN FLOWER SOLETTE MINETTE NOVA SUPER 28X, PRO SER is a medical device that received FDA 510(k) clearance on 1985-07-05. The listed applicant is Applied Science, Inc.. The 510(k) number is K851408.
When did SUN FLOWER SOLETTE MINETTE NOVA SUPER 28X, PRO SER receive FDA 510(k) clearance?
SUN FLOWER SOLETTE MINETTE NOVA SUPER 28X, PRO SER received FDA 510(k) clearance on 1985-07-05, under 510(k) number K851408.
Who is the listed applicant for SUN FLOWER SOLETTE MINETTE NOVA SUPER 28X, PRO SER?
The FDA 510(k) record lists Applied Science, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUN FLOWER SOLETTE MINETTE NOVA SUPER 28X, PRO SER?
The FDA product code for SUN FLOWER SOLETTE MINETTE NOVA SUPER 28X, PRO SER is FTC.
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.
Related Devices (Code: FTC)
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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