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FDA 510(k)

MUSTANG

K-Number: K954376 · 1995-12-08

ApplicantTemco, Inc.
Decision Date1995-12-08
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MUSTANG is the device name listed in this FDA 510(k) record. The listed applicant is Temco, Inc.. It received FDA 510(k) clearance on 1995-12-08 under 510(k) number K954376. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MUSTANG?

MUSTANG is a medical device that received FDA 510(k) clearance on 1995-12-08. The listed applicant is Temco, Inc.. The 510(k) number is K954376.

When did MUSTANG receive FDA 510(k) clearance?

MUSTANG received FDA 510(k) clearance on 1995-12-08, under 510(k) number K954376.

Who is the listed applicant for MUSTANG?

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

What is the FDA product code for MUSTANG?

The FDA product code for MUSTANG is IOR.

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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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