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FDA 510(k)

SPERTILITE PHOTOTHERAPY LAMP

K-Number: K862608 · 1986-08-06

ApplicantCooper-Hewitt Electric Co.
Decision Date1986-08-06
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent for Some Indications

Device Summary

SPERTILITE PHOTOTHERAPY LAMP is the device name listed in this FDA 510(k) record. The listed applicant is Cooper-Hewitt Electric Co.. It received FDA 510(k) clearance on 1986-08-06 under 510(k) number K862608. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the SPERTILITE PHOTOTHERAPY LAMP?

SPERTILITE PHOTOTHERAPY LAMP is a medical device that received FDA 510(k) clearance on 1986-08-06. The listed applicant is Cooper-Hewitt Electric Co.. The 510(k) number is K862608.

When did SPERTILITE PHOTOTHERAPY LAMP receive FDA 510(k) clearance?

SPERTILITE PHOTOTHERAPY LAMP received FDA 510(k) clearance on 1986-08-06, under 510(k) number K862608.

Who is the listed applicant for SPERTILITE PHOTOTHERAPY LAMP?

The FDA 510(k) record lists Cooper-Hewitt Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPERTILITE PHOTOTHERAPY LAMP?

The FDA product code for SPERTILITE PHOTOTHERAPY LAMP is FTC.

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Other records listing Cooper-Hewitt Electric Co. as applicant

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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.

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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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