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FDA 510(k)

RAINBOW, RAINBOW LIGHT,RAINBOW BLUE, RAINBOW PLUS

K-Number: K070338 · 2007-08-28

ApplicantRainbow Communications, Inc.
Decision Date2007-08-28
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RAINBOW, RAINBOW LIGHT,RAINBOW BLUE, RAINBOW PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Rainbow Communications, Inc.. It received FDA 510(k) clearance on 2007-08-28 under 510(k) number K070338. 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 RAINBOW, RAINBOW LIGHT,RAINBOW BLUE, RAINBOW PLUS?

RAINBOW, RAINBOW LIGHT,RAINBOW BLUE, RAINBOW PLUS is a medical device that received FDA 510(k) clearance on 2007-08-28. The listed applicant is Rainbow Communications, Inc.. The 510(k) number is K070338.

When did RAINBOW, RAINBOW LIGHT,RAINBOW BLUE, RAINBOW PLUS receive FDA 510(k) clearance?

RAINBOW, RAINBOW LIGHT,RAINBOW BLUE, RAINBOW PLUS received FDA 510(k) clearance on 2007-08-28, under 510(k) number K070338.

Who is the listed applicant for RAINBOW, RAINBOW LIGHT,RAINBOW BLUE, RAINBOW PLUS?

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

What is the FDA product code for RAINBOW, RAINBOW LIGHT,RAINBOW BLUE, RAINBOW PLUS?

The FDA product code for RAINBOW, RAINBOW LIGHT,RAINBOW BLUE, RAINBOW PLUS is ILY.

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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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