Atlas FDA

LITHOSTAR

FDA premarket approval P870018/S005 · decided 1992-02-05

Approval details

PMA number
P870018
Supplement
S005
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
LITHOSTAR
Generic name
Lithotriptor, extracorporeal shock-wave, urological
Applicant
Siemens Corp.
Date received
1991-10-02
Decision date
1992-02-05
Days to decision
126 days
Decision code
APRL
Product code
LNS
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Iselin, NJ

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510(k) clearances by this applicant

RecordFirmDate
DIMENSION VISTA DIGITOXIN CALIBRATOR - DGTX CAL (K103360)Siemens Corp.2010-12-17
KOORDINANT ANGIOGRAPHIC AND OPERATING ROOM MODEL X-RAY TABLE FAMILY (K993947)Siemens Corp.1999-12-21
AX WORKSTATION DR-VIEWER SOFTWARE OPTION (K992925)Siemens Corp.1999-11-23
HIGH ENDS GRADIENTS/MAGNETOM SYMPHONY SYSTEM (K991652)Siemens Corp.1999-08-03
SOMATOM PLUS 4 WITH SLIDING GANTRY OPTION (K991600)Siemens Corp.1999-06-09
FUNCTIONAL MRI PACKAGE FOR MAGETETOM VISION MR (K984221)Siemens Corp.1999-02-12
PERFUSION PACKAGE FOR MAGNETOM VISION AND SYMPHONY SYSTEMS (K984224)Siemens Corp.1999-02-02
PERFUSION CT (COMPUTED TOMOGRAPHY) SOFTWARE PACKAGE (K982536)Siemens Corp.1998-11-24