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FDA 510(k)

EMPI MODEL 712, LOGIX(TM), NMS

K-Number: K864010 · 1986-12-02

ApplicantEmpi
Decision Date1986-12-02
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EMPI MODEL 712, LOGIX(TM), NMS is the device name listed in this FDA 510(k) record. The listed applicant is Empi. It received FDA 510(k) clearance on 1986-12-02 under 510(k) number K864010. 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 EMPI MODEL 712, LOGIX(TM), NMS?

EMPI MODEL 712, LOGIX(TM), NMS is a medical device that received FDA 510(k) clearance on 1986-12-02. The listed applicant is Empi. The 510(k) number is K864010.

When did EMPI MODEL 712, LOGIX(TM), NMS receive FDA 510(k) clearance?

EMPI MODEL 712, LOGIX(TM), NMS received FDA 510(k) clearance on 1986-12-02, under 510(k) number K864010.

Who is the listed applicant for EMPI MODEL 712, LOGIX(TM), NMS?

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

What is the FDA product code for EMPI MODEL 712, LOGIX(TM), NMS?

The FDA product code for EMPI MODEL 712, LOGIX(TM), NMS is IPF.

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Other records listing Empi 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.

K093324EMPI CONTINUUMK090922EMPI ACTIVE TRANSCUTANEOUS NERVE STIMULATORK072946HYBRESIS IONTOPHORESIS DRUG DELIVERY SYSTEMK070427DUPEL TRANSPORT IONTOPHORESIS SYSTEMK061650SELECT TENS, MODEL 4600SK041920INFINITY PLUS ELECTROTHERAPY SYSTEM

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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.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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