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FDA 510(k)

FLEXIBLE ILLUMINATOR 10

K-Number: K840373 · 1984-04-24

Decision Date1984-04-24
Product CodeFTF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FLEXIBLE ILLUMINATOR 10 is the device name listed in this FDA 510(k) record. The listed applicant is Suncoast Medical Manufacturers, Inc.. It received FDA 510(k) clearance on 1984-04-24 under 510(k) number K840373. The device is classified under product code FTF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXIBLE ILLUMINATOR 10?

FLEXIBLE ILLUMINATOR 10 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 K840373.

When did FLEXIBLE ILLUMINATOR 10 receive FDA 510(k) clearance?

FLEXIBLE ILLUMINATOR 10 received FDA 510(k) clearance on 1984-04-24, under 510(k) number K840373.

Who is the listed applicant for FLEXIBLE ILLUMINATOR 10?

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 10?

The FDA product code for FLEXIBLE ILLUMINATOR 10 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.

View all 31 devices →

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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