Magnivision, Inc.

FDA Regulatory Profile

Magnivision, Inc. appears in FDA public data with 0 recalls, 8 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 30, 1990.

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K900778ITEM #272 MAGNIF-EYES CONTACT LENS CASEMarch 30, 1990
K900777ITEM #273 CONTACT LENS CASESMarch 30, 1990
K897084CONFEES(R)+ CONTACT LENS HOLDERFebruary 28, 1990
K897085COMFEES(R) + CON-PAK(TM) LENS CASEFebruary 28, 1990
K890533ITEM #352/#CS352* CONTACT LENS CASESJune 23, 1989
K882384DELUXE CONTACT LENS HOLDER (HARD & SOFT) #283June 23, 1989
K872567SOFT CONTACT LENS REMOVERAugust 10, 1987
K872591HARD CONTACT LENS REMOVER. ITEM #289August 4, 1987