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FDA 510(k)

REJUVENIQUE MODEL #RJV10

K-Number: K011935 · 2001-08-08

ApplicantSalton, Inc.
Decision Date2001-08-08
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

REJUVENIQUE MODEL #RJV10 is the device name listed in this FDA 510(k) record. The listed applicant is Salton, Inc.. It received FDA 510(k) clearance on 2001-08-08 under 510(k) number K011935. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REJUVENIQUE MODEL #RJV10?

REJUVENIQUE MODEL #RJV10 is a medical device that received FDA 510(k) clearance on 2001-08-08. The listed applicant is Salton, Inc.. The 510(k) number is K011935.

When did REJUVENIQUE MODEL #RJV10 receive FDA 510(k) clearance?

REJUVENIQUE MODEL #RJV10 received FDA 510(k) clearance on 2001-08-08, under 510(k) number K011935.

Who is the listed applicant for REJUVENIQUE MODEL #RJV10?

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

What is the FDA product code for REJUVENIQUE MODEL #RJV10?

The FDA product code for REJUVENIQUE MODEL #RJV10 is NFO.

Related Clinical Trials

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Other records listing Salton, Inc. as applicant

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Official Source

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