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FDA 510(k)

NAVIGATOR & TRAVELER EVOKED POSTENTIAL PRODUCT

K-Number: K930328 · 1993-07-02

ApplicantBio-Logic Systems Corp.
Decision Date1993-07-02
Product CodeIKN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NAVIGATOR & TRAVELER EVOKED POSTENTIAL PRODUCT is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Logic Systems Corp.. It received FDA 510(k) clearance on 1993-07-02 under 510(k) number K930328. The device is classified under product code IKN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAVIGATOR & TRAVELER EVOKED POSTENTIAL PRODUCT?

NAVIGATOR & TRAVELER EVOKED POSTENTIAL PRODUCT is a medical device that received FDA 510(k) clearance on 1993-07-02. The listed applicant is Bio-Logic Systems Corp.. The 510(k) number is K930328.

When did NAVIGATOR & TRAVELER EVOKED POSTENTIAL PRODUCT receive FDA 510(k) clearance?

NAVIGATOR & TRAVELER EVOKED POSTENTIAL PRODUCT received FDA 510(k) clearance on 1993-07-02, under 510(k) number K930328.

Who is the listed applicant for NAVIGATOR & TRAVELER EVOKED POSTENTIAL PRODUCT?

The FDA 510(k) record lists Bio-Logic Systems Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NAVIGATOR & TRAVELER EVOKED POSTENTIAL PRODUCT?

The FDA product code for NAVIGATOR & TRAVELER EVOKED POSTENTIAL PRODUCT is IKN.

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Other records listing Bio-Logic Systems Corp. 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.

K122496AUDX PRO OTOACOUSTIC EMISSIONS MEASUREMENT SYSTEMK121512SCOUT SPORT OTOACOUSTIC EMISSIONS MEASUREMENT SYSTEMK073626BIO-LOGIC MASTER II EVOKED RESPONSE SYSTEMK061744COCHLEA-SCAN / COCHLEA-SCAN PLUSK052066CEEGRAPH/SLEEPSCAN NETLINK TRAVELERK031352BIO-LOGIC INSERT EARPHONES

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Related Devices (Code: IKN)

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.

K172743Natus VikingQuestNatus Neurology IncorporatedK163150ViMove2Dorsavi, Ltd.K162383Cadwell Sierra Summit, Cadwell Sierra AscentCadwell Industries, Inc.K123902PHYSICAL MONITORING REGISTRATION UNIT-S (PMRU-S)Oktx, LLCK123399MYOVISION 3.0 WIREFREE SYSTEMPrecision Biometrics, Inc.K113074CMAP PROMedical Technologies, Inc.

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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