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FDA 510(k)

DAVID BACK CLINIC SYSTEM

K-Number: K952163 · 1996-08-12

ApplicantKinetic Resources, Inc.
Decision Date1996-08-12
Product CodeISD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DAVID BACK CLINIC SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Kinetic Resources, Inc.. It received FDA 510(k) clearance on 1996-08-12 under 510(k) number K952163. The device is classified under product code ISD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAVID BACK CLINIC SYSTEM?

DAVID BACK CLINIC SYSTEM is a medical device that received FDA 510(k) clearance on 1996-08-12. The listed applicant is Kinetic Resources, Inc.. The 510(k) number is K952163.

When did DAVID BACK CLINIC SYSTEM receive FDA 510(k) clearance?

DAVID BACK CLINIC SYSTEM received FDA 510(k) clearance on 1996-08-12, under 510(k) number K952163.

Who is the listed applicant for DAVID BACK CLINIC SYSTEM?

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

What is the FDA product code for DAVID BACK CLINIC SYSTEM?

The FDA product code for DAVID BACK CLINIC SYSTEM is ISD.

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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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