Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

OSCAR COLOR VISION TESTER

K-Number: K831074 · 1983-04-28

ApplicantCarl Zeiss, Inc.
Decision Date1983-04-28
Product CodeHIT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OSCAR COLOR VISION TESTER is the device name listed in this FDA 510(k) record. The listed applicant is Carl Zeiss, Inc.. It received FDA 510(k) clearance on 1983-04-28 under 510(k) number K831074. 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 OSCAR COLOR VISION TESTER?

OSCAR COLOR VISION TESTER is a medical device that received FDA 510(k) clearance on 1983-04-28. The listed applicant is Carl Zeiss, Inc.. The 510(k) number is K831074.

When did OSCAR COLOR VISION TESTER receive FDA 510(k) clearance?

OSCAR COLOR VISION TESTER received FDA 510(k) clearance on 1983-04-28, under 510(k) number K831074.

Who is the listed applicant for OSCAR COLOR VISION TESTER?

The FDA 510(k) record lists Carl Zeiss, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OSCAR COLOR VISION TESTER?

The FDA product code for OSCAR 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Carl Zeiss, 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.

K013402VISULAS 532SK003885VISULAS YAG IIK993357IOLMASTERK983868OPMI TWINER SURGICAL MICROSCOPEK965139SURGICAL MICROSCOPE NAVIGATOR (SMN) SYSTEM/SURGICAL TOOL NAVIGATOR (STN) SYSTEMK961380CPC PROBE

View all 44 devices →

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.

↑