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FDA 510(k)

HMP 4000 INTERFERENTIAL STIMULATOR

K-Number: K924961 · 1993-02-25

Decision Date1993-02-25
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

HMP 4000 INTERFERENTIAL STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Hmp 4000, Inc.. It received FDA 510(k) clearance on 1993-02-25 under 510(k) number K924961. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HMP 4000 INTERFERENTIAL STIMULATOR?

HMP 4000 INTERFERENTIAL STIMULATOR is a medical device that received FDA 510(k) clearance on 1993-02-25. The listed applicant is Hmp 4000, Inc.. The 510(k) number is K924961.

When did HMP 4000 INTERFERENTIAL STIMULATOR receive FDA 510(k) clearance?

HMP 4000 INTERFERENTIAL STIMULATOR received FDA 510(k) clearance on 1993-02-25, under 510(k) number K924961.

Who is the listed applicant for HMP 4000 INTERFERENTIAL STIMULATOR?

The FDA 510(k) record lists Hmp 4000, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HMP 4000 INTERFERENTIAL STIMULATOR?

The FDA product code for HMP 4000 INTERFERENTIAL STIMULATOR is LIH.

Related Clinical Trials

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.

Related Devices (Code: LIH)

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.

Official Source

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