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FDA 510(k)

STP COMPLETE MODULE SET

K-Number: K892425 · 1990-03-23

ApplicantLeibinger & Fischer , Ltd.
Decision Date1990-03-23
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

STP COMPLETE MODULE SET is the device name listed in this FDA 510(k) record. The listed applicant is Leibinger & Fischer , Ltd.. It received FDA 510(k) clearance on 1990-03-23 under 510(k) number K892425. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STP COMPLETE MODULE SET?

STP COMPLETE MODULE SET is a medical device that received FDA 510(k) clearance on 1990-03-23. The listed applicant is Leibinger & Fischer , Ltd.. The 510(k) number is K892425.

When did STP COMPLETE MODULE SET receive FDA 510(k) clearance?

STP COMPLETE MODULE SET received FDA 510(k) clearance on 1990-03-23, under 510(k) number K892425.

Who is the listed applicant for STP COMPLETE MODULE SET?

The FDA 510(k) record lists Leibinger & Fischer , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STP COMPLETE MODULE SET?

The FDA product code for STP COMPLETE MODULE SET is IYE.

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 Leibinger & Fischer , Ltd. 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.

K896450NEURO N 50 LESION GENERATOR

Related Devices (Code: IYE)

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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