ClearanceBrief
Company ยท US

Interlace Medical, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2008 to 2011. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
HIHHysteroscope (And Accessories)6
GCJLaparoscope, General & Plastic Surgery1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 2, 2011K103741SURGISURE TISSUE REMOVAL SYSTEM
Interlace Medical, Inc.
GCJ
Oct 15, 2010K102686MYOSURE ROD LENS SCOPE SEALS
Interlace Medical, Inc.
HIH
Mar 30, 2010K100559MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEM
Interlace Medical, Inc.
HIH
Oct 23, 2009K091100MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEM
Interlace Medical, Inc.
HIH
Aug 21, 2009K091465MYOSURE ROD LENS HYSTEROSCOPE
Interlace Medical, Inc.
HIH
Jul 23, 2008K081070INTERLACE MEDICAL OPERATIVE HYSTEROSCOPY SYSTEM
Interlace Medical, Inc.
HIH
Apr 17, 2008K073690INTERLACE MEDICAL HYSTEROSCOPIC MORCELLATION SYSTEM
Interlace Medical, Inc.
HIH

Latest recalls

DateFirm and productCodeLinked 510(k)
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