Pajunk GmbH is one of 5538 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pajunk GmbH - FDA 510(k) Cleared Devices
Recent clearances: SONO TAP, TUOHY SONO, CHIBA SONO, EPISPIN, EPISPIN II SAFETY, EPISPIN II, EPISPIN I, EPISPIN IV
19
Total
19
Cleared
0
Denied
Pajunk GmbH has 19 FDA 510(k) cleared anesthesiology devices. Based in Washington, US.
Historical record: 19 cleared submissions from 1991 to 2012.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Product Service, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Pajunk GmbH
19 devices
Cleared
Feb 29, 2012
SONO TAP, TUOHY SONO
Anesthesiology
121d
Cleared
Nov 21, 2011
CHIBA SONO
Gastroenterology & Urology
21d
Cleared
Jun 02, 2006
EPISPIN, EPISPIN II SAFETY, EPISPIN II, EPISPIN I, EPISPIN IV
Anesthesiology
114d
Cleared
Jan 12, 2006
UNIPLEX NANOLINE CANNULA, PLEXOLONG NANOLINE SET, STIMULONG NANOLINE SET
Anesthesiology
48d
Cleared
Dec 13, 2005
ADAPTABLE MONOPOLAR ELECTRODES WITH CERAMIC TIP
General & Plastic Surgery
18d
Cleared
Dec 21, 2004
MODIFICATION TO: PLEXALONG SETS
Anesthesiology
53d
Cleared
Dec 21, 2004
MODIFICATION TO PAJUNK STIMULONG PLUS CATHETER SETS
Anesthesiology
39d
Cleared
Sep 07, 2004
PAJUNK TUOHY NEEDLES, QUINCKE NEEDLES, CHIBA NEEDLES & CRAWFORD NEEDLES
Anesthesiology
146d
Cleared
May 05, 2004
STIMULONG PLUS CATHETER SET MODEL, VARIOUS
Anesthesiology
222d
Cleared
Mar 05, 2004
PAJUNK MODULAR HANDLE INSTRUMENTS
General & Plastic Surgery
150d
Cleared
Mar 24, 2003
MODIFICATION TO PLEXOLONG SETS
Anesthesiology
179d
Cleared
Jun 11, 2002
PLEXOLONG SETS
Anesthesiology
274d