FDA 510(k)

REMINGTON TANFASTIC COUNTERTOP FACIAL TANNER

K-Number: K895409 · 1989-10-20

ApplicantRemington Products Company, LLC

Decision Date1989-10-20

Product CodeLEJ

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

REMINGTON TANFASTIC COUNTERTOP FACIAL TANNER is the device name listed in this FDA 510(k) record. The listed applicant is Remington Products Company, LLC. It received FDA 510(k) clearance on 1989-10-20 under 510(k) number K895409. The device is classified under product code LEJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REMINGTON TANFASTIC COUNTERTOP FACIAL TANNER?

REMINGTON TANFASTIC COUNTERTOP FACIAL TANNER is a medical device that received FDA 510(k) clearance on 1989-10-20. The listed applicant is Remington Products Company, LLC. The 510(k) number is K895409.

When did REMINGTON TANFASTIC COUNTERTOP FACIAL TANNER receive FDA 510(k) clearance?

REMINGTON TANFASTIC COUNTERTOP FACIAL TANNER received FDA 510(k) clearance on 1989-10-20, under 510(k) number K895409.

Who is the listed applicant for REMINGTON TANFASTIC COUNTERTOP FACIAL TANNER?

The FDA 510(k) record lists Remington Products Company, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REMINGTON TANFASTIC COUNTERTOP FACIAL TANNER?

The FDA product code for REMINGTON TANFASTIC COUNTERTOP FACIAL TANNER is LEJ.

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Other records listing Remington Products Company, LLC as applicant

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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.