ClearanceBrief
Company ยท US

Medical Engineering and Development Institute

FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 1990. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GCCDilator, Catheter2
DREDilator, Vessel, For Percutaneous Catheterization1
DYBIntroducer, Catheter1
GADRetractor1
LJTPort & Catheter, Implanted, Subcutaneous, Intravascular1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 24, 1990K902477WORKSTATION FEMORAL INTRAVASCULAR RETRIEVAL SET
Medical Engineering and Development Institute
DYB
Aug 23, 1990K902469BYRD DILATOR SHEATH SET - TEFLON
Medical Engineering and Development Institute
DRE
Aug 7, 1990K902502BYRD STAINLESS STEEL DILATOR
Medical Engineering and Development Institute
GCC
Apr 17, 1990K895030LIFE-LINE(TM) VASCULAR ACCESS SYSTEM
Medical Engineering and Development Institute
LJT
Jun 23, 1989K893480BYRD EXTRACTOR SET
Medical Engineering and Development Institute
GCC
Mar 22, 1989K890820LOCKING WIRE GUIDE STYLET
Medical Engineering and Development Institute
GAD

Latest recalls

DateFirm and productCodeLinked 510(k)
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