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FDA 510(k)

HYDRO PULSE MASSAGE

K-Number: K792641 · 1980-01-28

ApplicantHydro-Pulse Research, Inc.
Decision Date1980-01-28
Product CodeILJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HYDRO PULSE MASSAGE is the device name listed in this FDA 510(k) record. The listed applicant is Hydro-Pulse Research, Inc.. It received FDA 510(k) clearance on 1980-01-28 under 510(k) number K792641. The device is classified under product code ILJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYDRO PULSE MASSAGE?

HYDRO PULSE MASSAGE is a medical device that received FDA 510(k) clearance on 1980-01-28. The listed applicant is Hydro-Pulse Research, Inc.. The 510(k) number is K792641.

When did HYDRO PULSE MASSAGE receive FDA 510(k) clearance?

HYDRO PULSE MASSAGE received FDA 510(k) clearance on 1980-01-28, under 510(k) number K792641.

Who is the listed applicant for HYDRO PULSE MASSAGE?

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

What is the FDA product code for HYDRO PULSE MASSAGE?

The FDA product code for HYDRO PULSE MASSAGE is ILJ.

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Related Devices (Code: ILJ)

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.

K110994PARKER 500Arjohuntleigh, Inc.K082951IMMERSION HYDROBATHArjo Hospital Equipment ABK052479MBATH 1000 (60)Enneking Medical, Inc.K040772PACIFIC RECUMBENT HEIGHT-ADJUSTABLE BATH SYSTEMPenner Manufacturing, Inc.K012061SUPERIOR BATH, MODEL 6300Penner Manufacturing, Inc.K012057CASCADE BATH, MODEL 6900Penner Manufacturing, Inc.

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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