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FDA 510(k)

ELECTRO-LIGHT THERAPY

K-Number: K090250 · 2010-02-11

ApplicantHill Laboratories Co.
Decision Date2010-02-11
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ELECTRO-LIGHT THERAPY is the device name listed in this FDA 510(k) record. The listed applicant is Hill Laboratories Co.. It received FDA 510(k) clearance on 2010-02-11 under 510(k) number K090250. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRO-LIGHT THERAPY?

ELECTRO-LIGHT THERAPY is a medical device that received FDA 510(k) clearance on 2010-02-11. The listed applicant is Hill Laboratories Co.. The 510(k) number is K090250.

When did ELECTRO-LIGHT THERAPY receive FDA 510(k) clearance?

ELECTRO-LIGHT THERAPY received FDA 510(k) clearance on 2010-02-11, under 510(k) number K090250.

Who is the listed applicant for ELECTRO-LIGHT THERAPY?

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

What is the FDA product code for ELECTRO-LIGHT THERAPY?

The FDA product code for ELECTRO-LIGHT THERAPY is ILY.

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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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