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FDA 510(k)

DOT VISUAL ACVITY TEST 2000

K-Number: K833956 · 1984-01-04

ApplicantGood-Lite Co.
Decision Date1984-01-04
Product CodeHOX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DOT VISUAL ACVITY TEST 2000 is the device name listed in this FDA 510(k) record. The listed applicant is Good-Lite Co.. It received FDA 510(k) clearance on 1984-01-04 under 510(k) number K833956. The device is classified under product code HOX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOT VISUAL ACVITY TEST 2000?

DOT VISUAL ACVITY TEST 2000 is a medical device that received FDA 510(k) clearance on 1984-01-04. The listed applicant is Good-Lite Co.. The 510(k) number is K833956.

When did DOT VISUAL ACVITY TEST 2000 receive FDA 510(k) clearance?

DOT VISUAL ACVITY TEST 2000 received FDA 510(k) clearance on 1984-01-04, under 510(k) number K833956.

Who is the listed applicant for DOT VISUAL ACVITY TEST 2000?

The FDA 510(k) record lists Good-Lite Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DOT VISUAL ACVITY TEST 2000?

The FDA product code for DOT VISUAL ACVITY TEST 2000 is HOX.

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Other records listing Good-Lite Co. 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.

K842515SURGICAL HEADLIGHTK842135HI-LO FLOOR STANDING EXAM. LIGHT

Related Devices (Code: HOX)

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.

K100095CENTRAL VISION ANALYZER MODEL 1000Vimetrics,Llc.K944156HEINE LAMBDA 100Heine USA , Ltd.K881971OCCU-TECH VISION TESTApplied Vision Concepts, Inc.K883337PL 20/20 INFANT VISION TESTEROptimed Technologies, Inc.K882634VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLAREVistech Consultants, Inc.K881358PG CONSEN CONTRAST SENSITIVITY TESTING PROGRAMNeuroscientific Corp.

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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