FLEXIBLE ILLUMINATOR 15
K-Number: K840372 · 1984-04-24
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Device Summary
Frequently Asked Questions
What is the FLEXIBLE ILLUMINATOR 15?
FLEXIBLE ILLUMINATOR 15 is a medical device that received FDA 510(k) clearance on 1984-04-24. The listed applicant is Suncoast Medical Manufacturers, Inc.. The 510(k) number is K840372.
When did FLEXIBLE ILLUMINATOR 15 receive FDA 510(k) clearance?
FLEXIBLE ILLUMINATOR 15 received FDA 510(k) clearance on 1984-04-24, under 510(k) number K840372.
Who is the listed applicant for FLEXIBLE ILLUMINATOR 15?
The FDA 510(k) record lists Suncoast Medical Manufacturers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLEXIBLE ILLUMINATOR 15?
The FDA product code for FLEXIBLE ILLUMINATOR 15 is FTF.
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 Suncoast Medical Manufacturers, 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: FTF)
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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