ClearanceBrief
Company ยท US

Magnivision, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1987 to 1990. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
1recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
LRXCase, Contact Lens6
KYEInserter/Remover Contact Lens2
HQZFrame, Spectacle1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 30, 1990K900778ITEM #272 MAGNIF-EYES CONTACT LENS CASE
Magnivision, Inc.
LRX
Mar 30, 1990K900777ITEM #273 CONTACT LENS CASES
Magnivision, Inc.
LRX
Feb 28, 1990K897085COMFEES(R) + CON-PAK(TM) LENS CASE
Magnivision, Inc.
LRX
Feb 28, 1990K897084CONFEES(R)+ CONTACT LENS HOLDER
Magnivision, Inc.
LRX
Jun 23, 1989K890533ITEM #352/#CS352* CONTACT LENS CASES
Magnivision, Inc.
LRX
Jun 23, 1989K882384DELUXE CONTACT LENS HOLDER (HARD & SOFT) #283
Magnivision, Inc.
LRX
Aug 10, 1987K872567SOFT CONTACT LENS REMOVER
Magnivision, Inc.
KYE
Aug 4, 1987K872591HARD CONTACT LENS REMOVER. ITEM #289
Magnivision, Inc.
KYE

Latest recalls

DateFirm and productCodeLinked 510(k)
Feb 24, 2004Magnivision, Inc.
Product is Magnivision UltraLights reading glasses which have the dioptic power on the label and ''MAGNIVISION AN AMERICAN GREETINGS COMPANY Miramar, FL 33025''
Terminated
HQZNone listed
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