ClearanceBrief
Company · DE

Henke-Sass, Wolf GmbH

FDA 510(k) clearances and medical device recalls filed under this name, 1994 to 2018. 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
HIHHysteroscope (And Accessories)2
FAJCystoscope And Accessories, Flexible/Rigid1
FHOPneumoperitoneum Needle1
FMFSyringe, Piston1
GCJLaparoscope, General & Plastic Surgery1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 8, 2018K173070HSW Resection Instruments
Henke-Sass, Wolf GmbH, DE
HIH
Dec 7, 2017K171336Cystoscope 4.0mm autoclavable 0° WL 302mm; Hysteroscope 4.0mm autoclavable 0° WL 302mm; Cysto-Urethroscope Sheath 19 Fr.
Henke-Sass, Wolf GmbH, DE
FAJ
Nov 22, 2010K101547HENKE- SASS, WOLF PISTON SYRINGE (NORM-JET)
Henke-Sass, Wolf GmbH
FMF
Feb 6, 1996K952186HSW GMBH HYSTEROSCOPES & ACCESSORIES
Henke-Sass, Wolf GmbH, DE
HIH
Aug 10, 1994K943624ELMED PNEUMOPERITONEUM NEEDLES
Henke-Sass, Wolf GmbH, DE
FHO
May 16, 1994K941967HSW LAPAROSCOPE AND ACCESSORIES
Henke-Sass, Wolf GmbH, DE
GCJ

Latest recalls

DateFirm and productCodeLinked 510(k)
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