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FDA 510(k)

SAUNDERS ELECTRONIC INCLINOMETER

K-Number: K943898 · 1994-11-28

ApplicantThe Saunders Group
Decision Date1994-11-28
Product CodeKQX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SAUNDERS ELECTRONIC INCLINOMETER is the device name listed in this FDA 510(k) record. The listed applicant is The Saunders Group. It received FDA 510(k) clearance on 1994-11-28 under 510(k) number K943898. The device is classified under product code KQX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAUNDERS ELECTRONIC INCLINOMETER?

SAUNDERS ELECTRONIC INCLINOMETER is a medical device that received FDA 510(k) clearance on 1994-11-28. The listed applicant is The Saunders Group. The 510(k) number is K943898.

When did SAUNDERS ELECTRONIC INCLINOMETER receive FDA 510(k) clearance?

SAUNDERS ELECTRONIC INCLINOMETER received FDA 510(k) clearance on 1994-11-28, under 510(k) number K943898.

Who is the listed applicant for SAUNDERS ELECTRONIC INCLINOMETER?

The FDA 510(k) record lists The Saunders Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAUNDERS ELECTRONIC INCLINOMETER?

The FDA product code for SAUNDERS ELECTRONIC INCLINOMETER is KQX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing The Saunders Group as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K0017123D ACTIVETRAC

Related Devices (Code: KQX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K011827ORTELIUS 800Orthoscan , Ltd.K971079INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWAREInterlogics, Inc.K9623773D-SPINESkill Technologies, Inc.K961212SPINAL TOUCHFasstechK954647INCLINOMETERJ-Tech, Inc.K943929DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS)Greenleaf Medical Systems, Inc.

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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