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FDA 510(k)

ARISE, VIVRE DEBOUT

K-Number: K862305 · 1986-07-09

ApplicantNatco Corp.
Decision Date1986-07-09
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ARISE, VIVRE DEBOUT is the device name listed in this FDA 510(k) record. The listed applicant is Natco Corp.. It received FDA 510(k) clearance on 1986-07-09 under 510(k) number K862305. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARISE, VIVRE DEBOUT?

ARISE, VIVRE DEBOUT is a medical device that received FDA 510(k) clearance on 1986-07-09. The listed applicant is Natco Corp.. The 510(k) number is K862305.

When did ARISE, VIVRE DEBOUT receive FDA 510(k) clearance?

ARISE, VIVRE DEBOUT received FDA 510(k) clearance on 1986-07-09, under 510(k) number K862305.

Who is the listed applicant for ARISE, VIVRE DEBOUT?

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

What is the FDA product code for ARISE, VIVRE DEBOUT?

The FDA product code for ARISE, VIVRE DEBOUT is IPL.

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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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