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FDA 510(k)

FLEX CONTROLLED PHOTOTHERAPY EQUIPMENT

K-Number: K050695 · 2005-04-19

Decision Date2005-04-19
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FLEX CONTROLLED PHOTOTHERAPY EQUIPMENT is the device name listed in this FDA 510(k) record. The listed applicant is Daavlin Distributing Co.. It received FDA 510(k) clearance on 2005-04-19 under 510(k) number K050695. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEX CONTROLLED PHOTOTHERAPY EQUIPMENT?

FLEX CONTROLLED PHOTOTHERAPY EQUIPMENT is a medical device that received FDA 510(k) clearance on 2005-04-19. The listed applicant is Daavlin Distributing Co.. The 510(k) number is K050695.

When did FLEX CONTROLLED PHOTOTHERAPY EQUIPMENT receive FDA 510(k) clearance?

FLEX CONTROLLED PHOTOTHERAPY EQUIPMENT received FDA 510(k) clearance on 2005-04-19, under 510(k) number K050695.

Who is the listed applicant for FLEX CONTROLLED PHOTOTHERAPY EQUIPMENT?

The FDA 510(k) record lists Daavlin Distributing Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLEX CONTROLLED PHOTOTHERAPY EQUIPMENT?

The FDA product code for FLEX CONTROLLED PHOTOTHERAPY EQUIPMENT 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.

Other records listing Daavlin Distributing Co. 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 14 devices →

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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