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FDA 510(k)

COMPUTERIZED ORTHOPAEDIC PEDOTOPOGRAPHY MACHINE

K-Number: K881284 · 1988-07-21

ApplicantNathaniel Gould Diagnostics, Inc.
Decision Date1988-07-21
Product CodeJFC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

COMPUTERIZED ORTHOPAEDIC PEDOTOPOGRAPHY MACHINE is the device name listed in this FDA 510(k) record. The listed applicant is Nathaniel Gould Diagnostics, Inc.. It received FDA 510(k) clearance on 1988-07-21 under 510(k) number K881284. The device is classified under product code JFC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPUTERIZED ORTHOPAEDIC PEDOTOPOGRAPHY MACHINE?

COMPUTERIZED ORTHOPAEDIC PEDOTOPOGRAPHY MACHINE is a medical device that received FDA 510(k) clearance on 1988-07-21. The listed applicant is Nathaniel Gould Diagnostics, Inc.. The 510(k) number is K881284.

When did COMPUTERIZED ORTHOPAEDIC PEDOTOPOGRAPHY MACHINE receive FDA 510(k) clearance?

COMPUTERIZED ORTHOPAEDIC PEDOTOPOGRAPHY MACHINE received FDA 510(k) clearance on 1988-07-21, under 510(k) number K881284.

Who is the listed applicant for COMPUTERIZED ORTHOPAEDIC PEDOTOPOGRAPHY MACHINE?

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

What is the FDA product code for COMPUTERIZED ORTHOPAEDIC PEDOTOPOGRAPHY MACHINE?

The FDA product code for COMPUTERIZED ORTHOPAEDIC PEDOTOPOGRAPHY MACHINE is JFC.

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Related Devices (Code: JFC)

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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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