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FDA 510(k)

PERCUSS-O-FLEX FOOT & HAND MASSAGER

K-Number: K810354 · 1981-02-23

ApplicantModern Reflexology, Inc.
Decision Date1981-02-23
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PERCUSS-O-FLEX FOOT & HAND MASSAGER is the device name listed in this FDA 510(k) record. The listed applicant is Modern Reflexology, Inc.. It received FDA 510(k) clearance on 1981-02-23 under 510(k) number K810354. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERCUSS-O-FLEX FOOT & HAND MASSAGER?

PERCUSS-O-FLEX FOOT & HAND MASSAGER is a medical device that received FDA 510(k) clearance on 1981-02-23. The listed applicant is Modern Reflexology, Inc.. The 510(k) number is K810354.

When did PERCUSS-O-FLEX FOOT & HAND MASSAGER receive FDA 510(k) clearance?

PERCUSS-O-FLEX FOOT & HAND MASSAGER received FDA 510(k) clearance on 1981-02-23, under 510(k) number K810354.

Who is the listed applicant for PERCUSS-O-FLEX FOOT & HAND MASSAGER?

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

What is the FDA product code for PERCUSS-O-FLEX FOOT & HAND MASSAGER?

The FDA product code for PERCUSS-O-FLEX FOOT & HAND MASSAGER is ISA.

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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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