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)

CILCO ANTERIOR CHAMBER LENS

K-Number: K771933 · 1978-01-26

ApplicantCalifornia Intraocular Lens
Decision Date1978-01-26
Product CodeHQL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CILCO ANTERIOR CHAMBER LENS is the device name listed in this FDA 510(k) record. The listed applicant is California Intraocular Lens. It received FDA 510(k) clearance on 1978-01-26 under 510(k) number K771933. The device is classified under product code HQL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CILCO ANTERIOR CHAMBER LENS?

CILCO ANTERIOR CHAMBER LENS is a medical device that received FDA 510(k) clearance on 1978-01-26. The listed applicant is California Intraocular Lens. The 510(k) number is K771933.

When did CILCO ANTERIOR CHAMBER LENS receive FDA 510(k) clearance?

CILCO ANTERIOR CHAMBER LENS received FDA 510(k) clearance on 1978-01-26, under 510(k) number K771933.

Who is the listed applicant for CILCO ANTERIOR CHAMBER LENS?

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

What is the FDA product code for CILCO ANTERIOR CHAMBER LENS?

The FDA product code for CILCO ANTERIOR CHAMBER LENS is HQL.

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: HQL)

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.

K914311CHIROFLEX II LENS MICROSERT(TM)Chiron OphthalmicsK913626SOFTRANS INJECTORStaar Surgical Co.K842892NIDEK DIGITAL KERATOMETERNidek, Inc.K842504AMER. MEDICAL OPTICS DIGITAL KERATO-American Medical Optics

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.

↑