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FDA 510(k)

CAPRI APPLICATOR

K-Number: K092822 · 2009-11-03

ApplicantVivaray, Inc.
Decision Date2009-11-03
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CAPRI APPLICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Vivaray, Inc.. It received FDA 510(k) clearance on 2009-11-03 under 510(k) number K092822. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAPRI APPLICATOR?

CAPRI APPLICATOR is a medical device that received FDA 510(k) clearance on 2009-11-03. The listed applicant is Vivaray, Inc.. The 510(k) number is K092822.

When did CAPRI APPLICATOR receive FDA 510(k) clearance?

CAPRI APPLICATOR received FDA 510(k) clearance on 2009-11-03, under 510(k) number K092822.

Who is the listed applicant for CAPRI APPLICATOR?

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

What is the FDA product code for CAPRI APPLICATOR?

The FDA product code for CAPRI APPLICATOR is JAQ.

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Related Devices (Code: JAQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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