ClearanceBrief
Company ยท GR

Stierlen-Maquet AG

FDA 510(k) clearances and medical device recalls filed under this name, 1984 to 1997. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
JEBTable, Surgical With Orthopedic Accessories, Manual4
GDCTable, Operating-Room, Electrical3
FQOTable, Operating-Room, Ac-Powered2
BWNTable And Attachments, Operating-Room1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 14, 1997K970807MOBILE OPERATING TABLE 1132.01
Stierlen-Maquet AG, DE
GDC
Oct 12, 1993K926525BETASTAR 1131.02 MOBILE OPERATING TABLE
Stierlen-Maquet AG, DE
FQO
Jul 2, 1992K920890OPERATING TABLE SYSTEM-BETAMAQUET 1140
Stierlen-Maquet AG, GR
FQO
Sep 15, 1988K883613OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO.
Stierlen-Maquet AG, GR
GDC
Sep 17, 1987K873276EXTENSION DEVICE 1416
Stierlen-Maquet AG, GR
JEB
Sep 17, 1987K873275EXTENSION TABLE 1417
Stierlen-Maquet AG, GR
JEB
Sep 17, 1987K873274PLASTER TABLE 1418
Stierlen-Maquet AG, GR
JEB
Sep 17, 1987K873273ORTHOPAEDIC TABLE 1420
Stierlen-Maquet AG, GR
JEB
Sep 8, 1987K873272ENDOSCOPY TABLE 1532 ENDOSTAR
Stierlen-Maquet AG, GR
BWN
Sep 7, 1984K843134MOBILE OPERATING TABLE HEIDELBERGS 1130
Stierlen-Maquet AG
GDC

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes