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FDA 510(k)

INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWARE

K-Number: K971079 · 1997-07-09

ApplicantInterlogics, Inc.
Decision Date1997-07-09
Product CodeKQX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Interlogics, Inc.. It received FDA 510(k) clearance on 1997-07-09 under 510(k) number K971079. 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 INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWARE?

INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWARE is a medical device that received FDA 510(k) clearance on 1997-07-09. The listed applicant is Interlogics, Inc.. The 510(k) number is K971079.

When did INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWARE receive FDA 510(k) clearance?

INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWARE received FDA 510(k) clearance on 1997-07-09, under 510(k) number K971079.

Who is the listed applicant for INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWARE?

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

What is the FDA product code for INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWARE?

The FDA product code for INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWARE is KQX.

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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.

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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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