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FDA 510(k)

STIMTRAC II CATALOG NUMBER 78-8500

K-Number: K895671 · 1989-11-06

Decision Date1989-11-06
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STIMTRAC II CATALOG NUMBER 78-8500 is the device name listed in this FDA 510(k) record. The listed applicant is Stimtech Products. It received FDA 510(k) clearance on 1989-11-06 under 510(k) number K895671. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STIMTRAC II CATALOG NUMBER 78-8500?

STIMTRAC II CATALOG NUMBER 78-8500 is a medical device that received FDA 510(k) clearance on 1989-11-06. The listed applicant is Stimtech Products. The 510(k) number is K895671.

When did STIMTRAC II CATALOG NUMBER 78-8500 receive FDA 510(k) clearance?

STIMTRAC II CATALOG NUMBER 78-8500 received FDA 510(k) clearance on 1989-11-06, under 510(k) number K895671.

Who is the listed applicant for STIMTRAC II CATALOG NUMBER 78-8500?

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

What is the FDA product code for STIMTRAC II CATALOG NUMBER 78-8500?

The FDA product code for STIMTRAC II CATALOG NUMBER 78-8500 is IPF.

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.

Other records listing Stimtech Products 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.

Related Devices (Code: IPF)

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.

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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