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FDA 510(k)

TRAVELER LT

K-Number: K862690 · 1986-11-25

ApplicantBio-Logic Systems Corp.
Decision Date1986-11-25
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TRAVELER LT 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 1986-11-25 under 510(k) number K862690. The device is classified under product code GWF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRAVELER LT?

TRAVELER LT is a medical device that received FDA 510(k) clearance on 1986-11-25. The listed applicant is Bio-Logic Systems Corp.. The 510(k) number is K862690.

When did TRAVELER LT receive FDA 510(k) clearance?

TRAVELER LT received FDA 510(k) clearance on 1986-11-25, under 510(k) number K862690.

Who is the listed applicant for TRAVELER LT?

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 TRAVELER LT?

The FDA product code for TRAVELER LT is GWF.

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Other records listing Bio-Logic Systems Corp. as applicant

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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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