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FDA 510(k)

TCD OR TCD NEUROPATHY STAR

K-Number: K944234 · 1995-03-08

ApplicantJcm Management & Planning Co.
Decision Date1995-03-08
Product CodeGWI
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TCD OR TCD NEUROPATHY STAR is the device name listed in this FDA 510(k) record. The listed applicant is Jcm Management & Planning Co.. It received FDA 510(k) clearance on 1995-03-08 under 510(k) number K944234. The device is classified under product code GWI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TCD OR TCD NEUROPATHY STAR?

TCD OR TCD NEUROPATHY STAR is a medical device that received FDA 510(k) clearance on 1995-03-08. The listed applicant is Jcm Management & Planning Co.. The 510(k) number is K944234.

When did TCD OR TCD NEUROPATHY STAR receive FDA 510(k) clearance?

TCD OR TCD NEUROPATHY STAR received FDA 510(k) clearance on 1995-03-08, under 510(k) number K944234.

Who is the listed applicant for TCD OR TCD NEUROPATHY STAR?

The FDA 510(k) record lists Jcm Management & Planning Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TCD OR TCD NEUROPATHY STAR?

The FDA product code for TCD OR TCD NEUROPATHY STAR is GWI.

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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Related Devices (Code: GWI)

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.

K874300AESTHESIOMETEROrthopedic 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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