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FDA 510(k)

BIO-LOGIC AUTOMATIC EVENT ANALYSIS

K-Number: K951594 · 1995-08-22

ApplicantBio-Logic Systems Corp.
Decision Date1995-08-22
Product CodeOMB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

BIO-LOGIC AUTOMATIC EVENT ANALYSIS 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 1995-08-22 under 510(k) number K951594. The device is classified under product code OMB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIO-LOGIC AUTOMATIC EVENT ANALYSIS?

BIO-LOGIC AUTOMATIC EVENT ANALYSIS is a medical device that received FDA 510(k) clearance on 1995-08-22. The listed applicant is Bio-Logic Systems Corp.. The 510(k) number is K951594.

When did BIO-LOGIC AUTOMATIC EVENT ANALYSIS receive FDA 510(k) clearance?

BIO-LOGIC AUTOMATIC EVENT ANALYSIS received FDA 510(k) clearance on 1995-08-22, under 510(k) number K951594.

Who is the listed applicant for BIO-LOGIC AUTOMATIC EVENT ANALYSIS?

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 BIO-LOGIC AUTOMATIC EVENT ANALYSIS?

The FDA product code for BIO-LOGIC AUTOMATIC EVENT ANALYSIS is OMB.

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Related Devices (Code: OMB)

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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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