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FDA 510(k)

KARMA DISCOVERY, MODEL KP40

K-Number: K014127 · 2002-03-15

ApplicantVestil Manufacturing Corp.
Decision Date2002-03-15
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KARMA DISCOVERY, MODEL KP40 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 2002-03-15 under 510(k) number K014127. 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 KARMA DISCOVERY, MODEL KP40?

KARMA DISCOVERY, MODEL KP40 is a medical device that received FDA 510(k) clearance on 2002-03-15. The listed applicant is Vestil Manufacturing Corp.. The 510(k) number is K014127.

When did KARMA DISCOVERY, MODEL KP40 receive FDA 510(k) clearance?

KARMA DISCOVERY, MODEL KP40 received FDA 510(k) clearance on 2002-03-15, under 510(k) number K014127.

Who is the listed applicant for KARMA DISCOVERY, MODEL KP40?

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 KARMA DISCOVERY, MODEL KP40?

The FDA product code for KARMA DISCOVERY, MODEL KP40 is 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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