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FDA 510(k)

PHOTIC STIMULATOR MODELS 580-PSCOMP,PSCEEG,PSSTAL

K-Number: K874136 · 1988-03-25

ApplicantBio-Logic Systems Corp.
Decision Date1988-03-25
Product CodeGWE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PHOTIC STIMULATOR MODELS 580-PSCOMP,PSCEEG,PSSTAL 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 1988-03-25 under 510(k) number K874136. The device is classified under product code GWE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHOTIC STIMULATOR MODELS 580-PSCOMP,PSCEEG,PSSTAL?

PHOTIC STIMULATOR MODELS 580-PSCOMP,PSCEEG,PSSTAL is a medical device that received FDA 510(k) clearance on 1988-03-25. The listed applicant is Bio-Logic Systems Corp.. The 510(k) number is K874136.

When did PHOTIC STIMULATOR MODELS 580-PSCOMP,PSCEEG,PSSTAL receive FDA 510(k) clearance?

PHOTIC STIMULATOR MODELS 580-PSCOMP,PSCEEG,PSSTAL received FDA 510(k) clearance on 1988-03-25, under 510(k) number K874136.

Who is the listed applicant for PHOTIC STIMULATOR MODELS 580-PSCOMP,PSCEEG,PSSTAL?

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 PHOTIC STIMULATOR MODELS 580-PSCOMP,PSCEEG,PSSTAL?

The FDA product code for PHOTIC STIMULATOR MODELS 580-PSCOMP,PSCEEG,PSSTAL is GWE.

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Other records listing Bio-Logic Systems Corp. as applicant

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Related Devices (Code: GWE)

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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