Medical Device Manufacturer · US , Research Triangle Park , NC

Pilling Weck, Inc.

6 submissions · 6 cleared · Since 1994
6
Total
6
Cleared
0
Denied

Pilling Weck, Inc. has 6 FDA 510(k) cleared medical devices. Based in Research Triangle Park, US.

Historical record: 6 cleared submissions from 1994 to 1999. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Pilling Weck, Inc. Filter by specialty or product code using the sidebar.

6 devices
1–6 of 6
PILLING WECK SURGICAL Y STENT FORCEPS
K990547 · EOQ Bronchoscope (flexible Or Rigid) · Ear, Nose, Throat
Apr 1999 64d
VERSASTAT MULTIPOLAR SCISSORS AND CABLES
K974250 · GEI Electrosurgical, Cutting & Coagulation & Accessories · General & Plastic Surgery
Feb 1998 90d
BURKE CONGENITAL THORACOSCOPY INSTRUMENTS
K962771 · DWS Instruments, Surgical, Cardiovascular · Cardiovascular
Nov 1996 126d
HEMOCLIP ECOSYSTEM
K945520 · GCJ Laparoscope, General & Plastic Surgery · General & Plastic Surgery
Jan 1995 78d
PILLING WECK M-20 DISPOSABLE AUTOMATIC HEMOCLIP
K944552 · FZP Clip, Implantable · General & Plastic Surgery
Nov 1994 52d
VISISTAT STAPLER
K943719 · GDT Staple, Removable (skin) · General & Plastic Surgery
Aug 1994 23d
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All6 General & Plastic Surgery 4 Cardiovascular 1 Ear, Nose, Throat 1