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FDA 510(k)

HIPUSH HANDHELD MASSAGER

K-Number: K823927 · 1983-02-15

ApplicantNew Age Corp.
Decision Date1983-02-15
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HIPUSH HANDHELD MASSAGER is the device name listed in this FDA 510(k) record. The listed applicant is New Age Corp.. It received FDA 510(k) clearance on 1983-02-15 under 510(k) number K823927. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HIPUSH HANDHELD MASSAGER?

HIPUSH HANDHELD MASSAGER is a medical device that received FDA 510(k) clearance on 1983-02-15. The listed applicant is New Age Corp.. The 510(k) number is K823927.

When did HIPUSH HANDHELD MASSAGER receive FDA 510(k) clearance?

HIPUSH HANDHELD MASSAGER received FDA 510(k) clearance on 1983-02-15, under 510(k) number K823927.

Who is the listed applicant for HIPUSH HANDHELD MASSAGER?

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

What is the FDA product code for HIPUSH HANDHELD MASSAGER?

The FDA product code for HIPUSH HANDHELD MASSAGER is ISA.

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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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