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FDA 510(k)

INTERTRON 6000/6100

K-Number: K930186 · 1993-07-02

ApplicantWilliams Healthcare Systems, LLC
Decision Date1993-07-02
Product CodeIMI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

INTERTRON 6000/6100 is the device name listed in this FDA 510(k) record. The listed applicant is Williams Healthcare Systems, LLC. It received FDA 510(k) clearance on 1993-07-02 under 510(k) number K930186. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERTRON 6000/6100?

INTERTRON 6000/6100 is a medical device that received FDA 510(k) clearance on 1993-07-02. The listed applicant is Williams Healthcare Systems, LLC. The 510(k) number is K930186.

When did INTERTRON 6000/6100 receive FDA 510(k) clearance?

INTERTRON 6000/6100 received FDA 510(k) clearance on 1993-07-02, under 510(k) number K930186.

Who is the listed applicant for INTERTRON 6000/6100?

The FDA 510(k) record lists Williams Healthcare Systems, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTERTRON 6000/6100?

The FDA product code for INTERTRON 6000/6100 is IMI.

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 Williams Healthcare Systems, LLC 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.

K933443COMBI 2.5 INTERSEGMENTAL TRACTION TABLE

Related Devices (Code: IMI)

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.

K240788Ultrasound StimulatorJkh Health Co., Ltd.K230472Sonopuls 190Enraf-Nonius, B.V.K222098ManaSport+Manamed, Inc.K210284ManaSportManamed, Inc.K202788Sonomed IV, Sonomed VCarci Industria E Comercio DE Aparelhos Cirurgicos E OrtoK160378BRH-A2 Combined Ultrasound and Electric Field Stimulation (CUSEFS)Brh Medical , Ltd.

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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