ClearanceBrief
Company ยท US

Nidacon International AB

FDA 510(k) clearances and medical device recalls filed under this name, 1998 to 2014. Name variants (Inc, Corp, punctuation) are merged.

12510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
MQLMedia, Reproductive11
MQKLabware, Assisted Reproduction1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Feb 20, 2014K131145PROINSERT
Nidacon International AB
MQK
Jun 15, 2010K092107VITRIBLAST, THERMOBLAST, MODEL VB-010, TB-010
Nidacon International AB
MQL
Nov 8, 2002K023206SPERM CRYOPROTEC
Nidacon International AB
MQL
Aug 28, 2002K022443SPERMASSIST
Nidacon International AB
MQL
Aug 10, 2001K011607SPERMCATCH
Nidacon International AB
MQL
Aug 3, 2001K012123NIDOIL
Nidacon International AB
MQL
Jul 12, 2001K011606PURESPERM BUFFER
Nidacon International AB
MQL
Jun 28, 2001K011346READYSWIM
Nidacon International AB
MQL
Nov 21, 2000K002630PURESPERM WASH
Nidacon International AB
MQL
Nov 20, 2000K002623PURESPERM 40 AND PURESPERM 80
Nidacon International AB
MQL
Jan 14, 1999K984172MODIFICATION OF PURESPERM
Nidacon International AB
MQL
Jun 23, 1998K980814PURESPERM
Nidacon International AB
MQL

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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