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FDA 510(k)

MODEL 7320 VISUAL STIMULATOR

K-Number: K781461 · 1978-11-08

ApplicantLife-Tech Instruments, Inc.
Decision Date1978-11-08
Product CodeGWE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MODEL 7320 VISUAL STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Life-Tech Instruments, Inc.. It received FDA 510(k) clearance on 1978-11-08 under 510(k) number K781461. 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 MODEL 7320 VISUAL STIMULATOR?

MODEL 7320 VISUAL STIMULATOR is a medical device that received FDA 510(k) clearance on 1978-11-08. The listed applicant is Life-Tech Instruments, Inc.. The 510(k) number is K781461.

When did MODEL 7320 VISUAL STIMULATOR receive FDA 510(k) clearance?

MODEL 7320 VISUAL STIMULATOR received FDA 510(k) clearance on 1978-11-08, under 510(k) number K781461.

Who is the listed applicant for MODEL 7320 VISUAL STIMULATOR?

The FDA 510(k) record lists Life-Tech Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 7320 VISUAL STIMULATOR?

The FDA product code for MODEL 7320 VISUAL STIMULATOR is GWE.

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Other records listing Life-Tech Instruments, Inc. 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.

K812177LIFE-TECH #1857 PRESSURE/POLOT MODULEK812179LIFE-TECH #1753 BIOFEEDBACK TRAINERK812180LIFE-TECH #5102 VISULABK812178LIFE-TECH #'S 1106/1156 UROLABSK800112AMBLYOPIA TRAINERK790663MODEL 1750 STANDING URINAL

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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.

K221471E3 and ProfileDiagnosys, LLCK212936Vision Monitor- MonCvONEMetrovisionK211974LED PHOTIC SystemMicromed S.P.A.K211643Vision Monitor - MonpackONEMetrovisionK200705Nurochek SystemCryptych Pty, Ltd.K173936Natus Photic StimulatorNatus Medical Incorporated Dba Excel-Tech Ltd. (Xltek)

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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