Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

WAHL(R) FOOT COMFORT MASSAGER

K-Number: K940837 · 1994-06-09

Decision Date1994-06-09
Product CodeIRO
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

WAHL(R) FOOT COMFORT MASSAGER is the device name listed in this FDA 510(k) record. The listed applicant is Wahl Clipper Corp.. It received FDA 510(k) clearance on 1994-06-09 under 510(k) number K940837. The device is classified under product code IRO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the WAHL(R) FOOT COMFORT MASSAGER?

WAHL(R) FOOT COMFORT MASSAGER is a medical device that received FDA 510(k) clearance on 1994-06-09. The listed applicant is Wahl Clipper Corp.. The 510(k) number is K940837.

When did WAHL(R) FOOT COMFORT MASSAGER receive FDA 510(k) clearance?

WAHL(R) FOOT COMFORT MASSAGER received FDA 510(k) clearance on 1994-06-09, under 510(k) number K940837.

Who is the listed applicant for WAHL(R) FOOT COMFORT MASSAGER?

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

What is the FDA product code for WAHL(R) FOOT COMFORT MASSAGER?

The FDA product code for WAHL(R) FOOT COMFORT MASSAGER is IRO.

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 Wahl Clipper Corp. 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 8 devices →

Related Devices (Code: IRO)

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.

↑