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FDA 510(k)

INTEGRATOR

K-Number: K950646 · 1996-04-30

ApplicantMoyco Union Broach, Div., Moyco Technologies, Inc.
Decision Date1996-04-30
Product CodeLXM
DecisionSubstantially Equivalent

Device Summary

INTEGRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Moyco Union Broach, Div., Moyco Technologies, Inc.. It received FDA 510(k) clearance on 1996-04-30 under 510(k) number K950646. The device is classified under product code LXM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTEGRATOR?

INTEGRATOR is a medical device that received FDA 510(k) clearance on 1996-04-30. The listed applicant is Moyco Union Broach, Div., Moyco Technologies, Inc.. The 510(k) number is K950646.

When did INTEGRATOR receive FDA 510(k) clearance?

INTEGRATOR received FDA 510(k) clearance on 1996-04-30, under 510(k) number K950646.

Who is the listed applicant for INTEGRATOR?

The FDA 510(k) record lists Moyco Union Broach, Div., Moyco Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTEGRATOR?

The FDA product code for INTEGRATOR is LXM.

Related Clinical Trials

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Related Devices (Code: LXM)

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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