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)

DIGISCOPE OPHTHALMIC CAMERA

K-Number: K990205 · 1999-03-26

ApplicantEye Tel Imaging, Inc.
Decision Date1999-03-26
Product CodeHKI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DIGISCOPE OPHTHALMIC CAMERA is the device name listed in this FDA 510(k) record. The listed applicant is Eye Tel Imaging, Inc.. It received FDA 510(k) clearance on 1999-03-26 under 510(k) number K990205. The device is classified under product code HKI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGISCOPE OPHTHALMIC CAMERA?

DIGISCOPE OPHTHALMIC CAMERA is a medical device that received FDA 510(k) clearance on 1999-03-26. The listed applicant is Eye Tel Imaging, Inc.. The 510(k) number is K990205.

When did DIGISCOPE OPHTHALMIC CAMERA receive FDA 510(k) clearance?

DIGISCOPE OPHTHALMIC CAMERA received FDA 510(k) clearance on 1999-03-26, under 510(k) number K990205.

Who is the listed applicant for DIGISCOPE OPHTHALMIC CAMERA?

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

What is the FDA product code for DIGISCOPE OPHTHALMIC CAMERA?

The FDA product code for DIGISCOPE OPHTHALMIC CAMERA is HKI.

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

Related Devices (Code: HKI)

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.

K253176TearViewBeyond 700 Pty, Ltd.K251353Eyer 2Phelcom TechnologiesK252120Fundus On Phone Non Mydriatic (FOP NM-10)Remidio Innovative Solutions Private LimitedK250770Optina-4C (MHRC-C1N)Optina Diagnostics, Inc.K2436003nethra neo HD FA; 3nethra neo HDForus Health Pvt.LtdK250683Resolve Fundus CameraOptain Health, 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.

↑