Stierlen-Maquet AG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stierlen-Maquet AG - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Stierlen-Maquet AG has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.
Historical record: 10 cleared submissions from 1984 to 1997.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Stierlen-Maquet AG
10 devices
Cleared
Mar 14, 1997
MOBILE OPERATING TABLE 1132.01
General & Plastic Surgery
9d
Cleared
Oct 12, 1993
BETASTAR 1131.02 MOBILE OPERATING TABLE
General & Plastic Surgery
286d
Cleared
Jul 02, 1992
OPERATING TABLE SYSTEM-BETAMAQUET 1140
General & Plastic Surgery
141d
Cleared
Sep 15, 1988
OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO.
General & Plastic Surgery
24d
Cleared
Sep 17, 1987
ORTHOPAEDIC TABLE 1420
General & Plastic Surgery
31d
Cleared
Sep 17, 1987
PLASTER TABLE 1418
General & Plastic Surgery
31d
Cleared
Sep 17, 1987
EXTENSION TABLE 1417
General & Plastic Surgery
31d
Cleared
Sep 17, 1987
EXTENSION DEVICE 1416
General & Plastic Surgery
31d
Cleared
Sep 08, 1987
ENDOSCOPY TABLE 1532 ENDOSTAR
General & Plastic Surgery
22d
Cleared
Sep 07, 1984
MOBILE OPERATING TABLE HEIDELBERGS 1130
General & Plastic Surgery
29d