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FDA 510(k)

SUNLAMP

K-Number: K790167 · 1979-03-21

ApplicantKneilsly Group Ent.
Decision Date1979-03-21
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUNLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Kneilsly Group Ent.. It received FDA 510(k) clearance on 1979-03-21 under 510(k) number K790167. 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 SUNLAMP?

SUNLAMP is a medical device that received FDA 510(k) clearance on 1979-03-21. The listed applicant is Kneilsly Group Ent.. The 510(k) number is K790167.

When did SUNLAMP receive FDA 510(k) clearance?

SUNLAMP received FDA 510(k) clearance on 1979-03-21, under 510(k) number K790167.

Who is the listed applicant for SUNLAMP?

The FDA 510(k) record lists Kneilsly Group Ent. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUNLAMP?

The FDA product code for SUNLAMP is FTC.

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Related Devices (Code: FTC)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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