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FDA 510(k)

BALANCED CAST SOLE

K-Number: K760578 · 1976-09-27

ApplicantParke-Davis Co.
Decision Date1976-09-27
Product CodeIPG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BALANCED CAST SOLE is the device name listed in this FDA 510(k) record. The listed applicant is Parke-Davis Co.. It received FDA 510(k) clearance on 1976-09-27 under 510(k) number K760578. 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 BALANCED CAST SOLE?

BALANCED CAST SOLE is a medical device that received FDA 510(k) clearance on 1976-09-27. The listed applicant is Parke-Davis Co.. The 510(k) number is K760578.

When did BALANCED CAST SOLE receive FDA 510(k) clearance?

BALANCED CAST SOLE received FDA 510(k) clearance on 1976-09-27, under 510(k) number K760578.

Who is the listed applicant for BALANCED CAST SOLE?

The FDA 510(k) record lists Parke-Davis Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BALANCED CAST SOLE?

The FDA product code for BALANCED CAST SOLE is IPG.

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Related Devices (Code: IPG)

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K024279NESS CHILDREN SYSTEMNess-Neuromuscular Electrical Stimulation SystemsK790652TOGUARDTogard, Inc.K781363CAST SHOECutler BiomedicalK780617EQUALIZERBallert Orthopedic Corp.K760575ROCKER-SOLE CAST SANDALRichard'S Medical Equip., 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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