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FDA 510(k)

EBI FOOT MASSAGING PUMP

K-Number: K852264 · 1985-07-19

Decision Date1985-07-19
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EBI FOOT MASSAGING PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Electro-Biology, Inc.. It received FDA 510(k) clearance on 1985-07-19 under 510(k) number K852264. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EBI FOOT MASSAGING PUMP?

EBI FOOT MASSAGING PUMP is a medical device that received FDA 510(k) clearance on 1985-07-19. The listed applicant is Electro-Biology, Inc.. The 510(k) number is K852264.

When did EBI FOOT MASSAGING PUMP receive FDA 510(k) clearance?

EBI FOOT MASSAGING PUMP received FDA 510(k) clearance on 1985-07-19, under 510(k) number K852264.

Who is the listed applicant for EBI FOOT MASSAGING PUMP?

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

What is the FDA product code for EBI FOOT MASSAGING PUMP?

The FDA product code for EBI FOOT MASSAGING PUMP is IRP.

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.

Other records listing Electro-Biology, Inc. as applicant

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.

View all 28 devices →

Related Devices (Code: IRP)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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