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FDA 510(k)

INFRADERM; TOUCH 'N TONE PLUS

K-Number: K911727 · 1994-02-25

ApplicantConair Corp.
Decision Date1994-02-25
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

INFRADERM; TOUCH 'N TONE PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Conair Corp.. It received FDA 510(k) clearance on 1994-02-25 under 510(k) number K911727. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFRADERM; TOUCH 'N TONE PLUS?

INFRADERM; TOUCH 'N TONE PLUS is a medical device that received FDA 510(k) clearance on 1994-02-25. The listed applicant is Conair Corp.. The 510(k) number is K911727.

When did INFRADERM; TOUCH 'N TONE PLUS receive FDA 510(k) clearance?

INFRADERM; TOUCH 'N TONE PLUS received FDA 510(k) clearance on 1994-02-25, under 510(k) number K911727.

Who is the listed applicant for INFRADERM; TOUCH 'N TONE PLUS?

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

What is the FDA product code for INFRADERM; TOUCH 'N TONE PLUS?

The FDA product code for INFRADERM; TOUCH 'N TONE PLUS is ISA.

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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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