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FDA 510(k)

CHROMOPS FM-100 COLOR VISION TESTER

K-Number: K810700 · 1981-04-10

ApplicantVisidyne Corp.
Decision Date1981-04-10
Product CodeHIT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CHROMOPS FM-100 COLOR VISION TESTER is the device name listed in this FDA 510(k) record. The listed applicant is Visidyne Corp.. It received FDA 510(k) clearance on 1981-04-10 under 510(k) number K810700. The device is classified under product code HIT. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHROMOPS FM-100 COLOR VISION TESTER?

CHROMOPS FM-100 COLOR VISION TESTER is a medical device that received FDA 510(k) clearance on 1981-04-10. The listed applicant is Visidyne Corp.. The 510(k) number is K810700.

When did CHROMOPS FM-100 COLOR VISION TESTER receive FDA 510(k) clearance?

CHROMOPS FM-100 COLOR VISION TESTER received FDA 510(k) clearance on 1981-04-10, under 510(k) number K810700.

Who is the listed applicant for CHROMOPS FM-100 COLOR VISION TESTER?

The FDA 510(k) record lists Visidyne Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHROMOPS FM-100 COLOR VISION TESTER?

The FDA product code for CHROMOPS FM-100 COLOR VISION TESTER is HIT.

Related Clinical Trials

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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Other records listing Visidyne Corp. 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.

K811316TRISCAN, MODELS 38,40,41,43 & 45K810699PANTOPS M-2 ELECTROPHYSIOLOGY SYSTEM

Related Devices (Code: HIT)

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.

K903001SLIMCATH (TM)Gynopharma, Inc.K875026ANOMALOSCOPE PLATE TEST - 5 [APT-5]Lkc Technologies, Inc.K873908H.R.R. PSEUDOISOCHROMATIC COLOR BLINDNESS TEST BK.Richmond Products, Inc.K873911PSEUDO ISOCHROMATIC COLOR BLINDNESS TEST BOOK - 15Richmond Products, Inc.K844694TITMUS VISION TESTER IITitmus Optical, Inc.K844365COLOR VISION TESTERSLuneau Laboratories

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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