FDA 510(k)

ROCKER-SOLE CAST SANDAL

K-Number: K760575 · 1976-10-06

Decision Date1976-10-06

Product CodeIPG

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

ROCKER-SOLE CAST SANDAL is the device name listed in this FDA 510(k) record. The listed applicant is Richard'S Medical Equip., Inc.. It received FDA 510(k) clearance on 1976-10-06 under 510(k) number K760575. The device is classified under product code IPG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROCKER-SOLE CAST SANDAL?

ROCKER-SOLE CAST SANDAL is a medical device that received FDA 510(k) clearance on 1976-10-06. The listed applicant is Richard'S Medical Equip., Inc.. The 510(k) number is K760575.

When did ROCKER-SOLE CAST SANDAL receive FDA 510(k) clearance?

ROCKER-SOLE CAST SANDAL received FDA 510(k) clearance on 1976-10-06, under 510(k) number K760575.

Who is the listed applicant for ROCKER-SOLE CAST SANDAL?

The FDA 510(k) record lists Richard'S Medical Equip., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ROCKER-SOLE CAST SANDAL?

The FDA product code for ROCKER-SOLE CAST SANDAL is IPG.

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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.