Device Type ID | 4359 |
Device Name | Lens, Contact, (disposable) |
Regulation Description | Soft (hydrophilic) Contact Lens. |
Regulation Medical Specialty | Ophthalmic |
Review Panel | Ophthalmic |
Premarket Review | Office Of Device Evaluation (ODE) Division Of Ophthalmic And Ear, Nose And Throat Devices (DOED) Contact Lenses And Retinal Devices Branch (CLRD) |
Submission Type | 510(k) |
CFR Regulation Number | 886.5925 [🔎] |
FDA Device Classification | Class 2 Medical Device |
Product Code | MVN |
GMP Exempt | No |
Summary MR | Eligible |
Implanted Device | No |
Life Support Device | No |
Third Party Review | Eligible For Accredited Persons Program |
Device Type ID | 4359 |
Device | Lens, Contact, (disposable) |
Product Code | MVN |
FDA Device Classification | Class 2 Medical Device |
Regulation Description | Soft (hydrophilic) Contact Lens. |
CFR Regulation Number | 886.5925 [🔎] |
Premarket Reviews | ||
---|---|---|
Manufacturer | Decision | |
YUNG SHENG OPTICAL CO., LTD. | ||
SUBSTANTIALLY EQUIVALENT | 2 |
Device Problems | |
---|---|
Adverse Event Without Identified Device Or Use Problem | 44 |
Contact Lens | 4 |
Insufficient Information | 4 |
Torn Material | 2 |
Device Contaminated During Manufacture Or Shipping | 1 |
Appropriate Term/Code Not Available | 1 |
Improper Or Incorrect Procedure Or Method | 1 |
Total Device Problems | 57 |
Recalls | |||
---|---|---|---|
Manufacturer | Recall Class | Date Posted | |
1 | CooperVision Inc. | III | Apr-25-2018 |
2 | Johnson & Johnson Vision Care, Inc. | II | Mar-27-2018 |