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)

COMFEES(R) + CON-PAK(TM) LENS CASE

K-Number: K897085 · 1990-02-28

ApplicantMagnivision, Inc.
Decision Date1990-02-28
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

COMFEES(R) + CON-PAK(TM) LENS CASE is the device name listed in this FDA 510(k) record. The listed applicant is Magnivision, Inc.. It received FDA 510(k) clearance on 1990-02-28 under 510(k) number K897085. 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 COMFEES(R) + CON-PAK(TM) LENS CASE?

COMFEES(R) + CON-PAK(TM) LENS CASE is a medical device that received FDA 510(k) clearance on 1990-02-28. The listed applicant is Magnivision, Inc.. The 510(k) number is K897085.

When did COMFEES(R) + CON-PAK(TM) LENS CASE receive FDA 510(k) clearance?

COMFEES(R) + CON-PAK(TM) LENS CASE received FDA 510(k) clearance on 1990-02-28, under 510(k) number K897085.

Who is the listed applicant for COMFEES(R) + CON-PAK(TM) LENS CASE?

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

What is the FDA product code for COMFEES(R) + CON-PAK(TM) LENS CASE?

The FDA product code for COMFEES(R) + CON-PAK(TM) LENS CASE 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 Magnivision, 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.

K900778ITEM #272 MAGNIF-EYES CONTACT LENS CASEK900777ITEM #273 CONTACT LENS CASESK897084CONFEES(R)+ CONTACT LENS HOLDERK890533ITEM #352/#CS352* CONTACT LENS CASESK882384DELUXE CONTACT LENS HOLDER (HARD & SOFT) #283K872567SOFT CONTACT LENS REMOVER

View all 8 devices →

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.

↑