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)

TITMUS VISION TESTER II

K-Number: K844694 · 1985-01-22

ApplicantTitmus Optical, Inc.
Decision Date1985-01-22
Product CodeHIT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TITMUS VISION TESTER II is the device name listed in this FDA 510(k) record. The listed applicant is Titmus Optical, Inc.. It received FDA 510(k) clearance on 1985-01-22 under 510(k) number K844694. 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 TITMUS VISION TESTER II?

TITMUS VISION TESTER II is a medical device that received FDA 510(k) clearance on 1985-01-22. The listed applicant is Titmus Optical, Inc.. The 510(k) number is K844694.

When did TITMUS VISION TESTER II receive FDA 510(k) clearance?

TITMUS VISION TESTER II received FDA 510(k) clearance on 1985-01-22, under 510(k) number K844694.

Who is the listed applicant for TITMUS VISION TESTER II?

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

What is the FDA product code for TITMUS VISION TESTER II?

The FDA product code for TITMUS VISION TESTER II 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 Titmus Optical, 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.

K843096CRISTY/COTEK832762MILLER/NADLER GLARE TESTER

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.K844365COLOR VISION TESTERSLuneau LaboratoriesK832843OSCAR COLOUR VISION TESTERKeeler Instruments, Inc.

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.

↑