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)

RETCAM PORTABLE OPHTHALMIC IMAGING SYSTEM, MODEL RCP

K-Number: K083771 · 2009-01-30

ApplicantClarity Medical Systems
Decision Date2009-01-30
Product CodeHKI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RETCAM PORTABLE OPHTHALMIC IMAGING SYSTEM, MODEL RCP is the device name listed in this FDA 510(k) record. The listed applicant is Clarity Medical Systems. It received FDA 510(k) clearance on 2009-01-30 under 510(k) number K083771. 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 RETCAM PORTABLE OPHTHALMIC IMAGING SYSTEM, MODEL RCP?

RETCAM PORTABLE OPHTHALMIC IMAGING SYSTEM, MODEL RCP is a medical device that received FDA 510(k) clearance on 2009-01-30. The listed applicant is Clarity Medical Systems. The 510(k) number is K083771.

When did RETCAM PORTABLE OPHTHALMIC IMAGING SYSTEM, MODEL RCP receive FDA 510(k) clearance?

RETCAM PORTABLE OPHTHALMIC IMAGING SYSTEM, MODEL RCP received FDA 510(k) clearance on 2009-01-30, under 510(k) number K083771.

Who is the listed applicant for RETCAM PORTABLE OPHTHALMIC IMAGING SYSTEM, MODEL RCP?

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

What is the FDA product code for RETCAM PORTABLE OPHTHALMIC IMAGING SYSTEM, MODEL RCP?

The FDA product code for RETCAM PORTABLE OPHTHALMIC IMAGING SYSTEM, MODEL RCP 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

Other records listing Clarity Medical Systems 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.

K102859RETCAM 3 OPTHALMIC IMAGING SYSTEMK090326RET CAM II, RETCAM 3 AND RETCAM SHUTTLE AND PORTABLE OPHTHALMIC IMAGING SYSTEMSK081858RETCAM 3 OPHTHALMIC IMAGING SYSTEM

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.

↑