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FDA 510(k)

TAN MODEL I

K-Number: K853046 · 1985-08-07

ApplicantPhilip Munsterman Tan, Inc.
Decision Date1985-08-07
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TAN MODEL I is the device name listed in this FDA 510(k) record. The listed applicant is Philip Munsterman Tan, Inc.. It received FDA 510(k) clearance on 1985-08-07 under 510(k) number K853046. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAN MODEL I?

TAN MODEL I is a medical device that received FDA 510(k) clearance on 1985-08-07. The listed applicant is Philip Munsterman Tan, Inc.. The 510(k) number is K853046.

When did TAN MODEL I receive FDA 510(k) clearance?

TAN MODEL I received FDA 510(k) clearance on 1985-08-07, under 510(k) number K853046.

Who is the listed applicant for TAN MODEL I?

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

What is the FDA product code for TAN MODEL I?

The FDA product code for TAN MODEL I is FTC.

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Related Devices (Code: FTC)

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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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