HMP 4000 INTERFERENTIAL STIMULATOR
K-Number: K924961 · 1993-02-25
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Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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