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FDA 510(k)

FRONTIER MODEL X5

K-Number: K030783 · 2003-04-04

ApplicantVestil Manufacturing Corp.
Decision Date2003-04-04
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FRONTIER MODEL X5 is the device name listed in this FDA 510(k) record. The listed applicant is Vestil Manufacturing Corp.. It received FDA 510(k) clearance on 2003-04-04 under 510(k) number K030783. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FRONTIER MODEL X5?

FRONTIER MODEL X5 is a medical device that received FDA 510(k) clearance on 2003-04-04. The listed applicant is Vestil Manufacturing Corp.. The 510(k) number is K030783.

When did FRONTIER MODEL X5 receive FDA 510(k) clearance?

FRONTIER MODEL X5 received FDA 510(k) clearance on 2003-04-04, under 510(k) number K030783.

Who is the listed applicant for FRONTIER MODEL X5?

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

What is the FDA product code for FRONTIER MODEL X5?

The FDA product code for FRONTIER MODEL X5 is ITI.

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Other records listing Vestil Manufacturing Corp. as applicant

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Related Devices (Code: ITI)

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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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