ClearanceBrief
Company ยท US

Pilling Weck Surgical

FDA 510(k) clearances and medical device recalls filed under this name, 1998 to 2000. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DXCClamp, Vascular1
JEKForceps, Biopsy, Bronchoscope (Rigid)1
JOHTube Tracheostomy And Tube Cuff1
KNQDilator, Esophageal1
MWSStabilizer, Heart1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 13, 2000K992476PILLING WECK SURGICAL HEART STABILIZER REMOVABLE PADS
Pilling Weck Surgical
MWS
Mar 23, 2000K992174PILLING WECK SURGICAL AORTIC SPOON-JAW CLAMP
Pilling Weck Surgical
DXC
May 17, 1999K990935JACKSON ESOPHAGEAL DILATOR
Pilling Weck Surgical
KNQ
May 14, 1999K990561OPTICAL FORCEPS
Pilling Weck Surgical
JEK
Oct 23, 1998K982128SHIKANI-FRENCH SPEAKING VALVE
Pilling Weck Surgical
JOH

Latest recalls

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