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)

CONTACT LENS CASE FOR SOFT LENSES

K-Number: K840692 · 1984-06-07

ApplicantOptimum Manufacturers, Inc.
Decision Date1984-06-07
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CONTACT LENS CASE FOR SOFT LENSES is the device name listed in this FDA 510(k) record. The listed applicant is Optimum Manufacturers, Inc.. It received FDA 510(k) clearance on 1984-06-07 under 510(k) number K840692. The device is classified under product code LRX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTACT LENS CASE FOR SOFT LENSES?

CONTACT LENS CASE FOR SOFT LENSES is a medical device that received FDA 510(k) clearance on 1984-06-07. The listed applicant is Optimum Manufacturers, Inc.. The 510(k) number is K840692.

When did CONTACT LENS CASE FOR SOFT LENSES receive FDA 510(k) clearance?

CONTACT LENS CASE FOR SOFT LENSES received FDA 510(k) clearance on 1984-06-07, under 510(k) number K840692.

Who is the listed applicant for CONTACT LENS CASE FOR SOFT LENSES?

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

What is the FDA product code for CONTACT LENS CASE FOR SOFT LENSES?

The FDA product code for CONTACT LENS CASE FOR SOFT LENSES is LRX.

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 Optimum Manufacturers, 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.

K841163CONTACT LENS INSERTER/REMOVERK840691CONTACT LENS CASE FOR RIGID GAS PERMA

Related Devices (Code: LRX)

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.

K252175LANDR Contact LENS CaseFourth Axis, LLCK250495MINI VP1 (PL67_F); MINI VP1 (PL61_F)Avizor S.A.K240095CAREUS Contact Lens Case (Model 1, Model 2, Model 3, Model 4, Model 5, Model 6)Shanghai Care US Medical Product Co., Ltd.K231123Phoenix Contact Lens Case - dome top flat pack (CL-01); Phoenix Contact Lens Case - classic flat pack (CL-02); Phoenix Contact Lens Case - sunglass shape flat pack (CL-03)Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd.K173538Clear Care Cleaning & Disinfecting Solution, AOCup Lens Case with AODiscAlcon Laboratories, Inc.K172925Contact Lens Case, Model: A-1, B-1P L Overseas Limited

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.

↑