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FDA 510(k)

PHOTOTHERAPY LIGHT

K-Number: K760872 · 1976-11-02

ApplicantAir-Shields, Inc.
Decision Date1976-11-02
Product CodeLBI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PHOTOTHERAPY LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Air-Shields, Inc.. It received FDA 510(k) clearance on 1976-11-02 under 510(k) number K760872. The device is classified under product code LBI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHOTOTHERAPY LIGHT?

PHOTOTHERAPY LIGHT is a medical device that received FDA 510(k) clearance on 1976-11-02. The listed applicant is Air-Shields, Inc.. The 510(k) number is K760872.

When did PHOTOTHERAPY LIGHT receive FDA 510(k) clearance?

PHOTOTHERAPY LIGHT received FDA 510(k) clearance on 1976-11-02, under 510(k) number K760872.

Who is the listed applicant for PHOTOTHERAPY LIGHT?

The FDA 510(k) record lists Air-Shields, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHOTOTHERAPY LIGHT?

The FDA product code for PHOTOTHERAPY LIGHT is LBI.

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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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