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FETAL ACOUSTIC STIMULATOR

FDA premarket approval P870025/S008 · decided 2006-03-02

Approval details

PMA number
P870025
Supplement
S008
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
FETAL ACOUSTIC STIMULATOR
Generic name
Stimulator, fetal, acoustic
Applicant
Ge Medical Systems, Inc.
Date received
2005-08-01
Decision date
2006-03-02
Days to decision
213 days
Decision code
APPR
Product code
MCP
Advisory committee
Obstetrics/Gynecology
Expedited review
No
Location
Tampa, FL
Statement
APPROVAL FOR VENDOR CHANGES FOR THE FOLLOWING COMPONENTS: DIE CAST FRAME AND PRINTED CIRCUIT BOARD (PCB) AND A CHANGE IN ADHESIVE MATERIAL.

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510(k) clearances by this applicant

RecordFirmDate
GE LIGHTSPEED ACT FP16 (K091673)Ge Medical Systems, Inc.2009-06-24
GE LIGHTSPEED RT16 / LIGHTSPEED XTRA V2 CT SYSTEM (AKA GE LIGHTSPEED RT16 / LIGHTSPEED XTRA CT SYSTEM (K082104)Ge Medical Systems, Inc.2008-09-02
GE SIGNA EXCITE 1.5T 6 CHANNEL PHASED ARRAY FLEX COIL, GE SIGNA EXCITE 3.0T 6 CHANNEL PHASED ARRAY FLEX COIL (K042844)Ge Medical Systems, Inc.2004-11-03
INNOVA 4100, INNOVA 3100 (K042053)Ge Medical Systems, Inc.2004-08-26
SENOGRAPHIC STEREO (K040125)Ge Medical Systems, Inc.2004-04-19
DIGITAL FLUOROSCOPIC IMAGING SYSTEM, MODEL INNOVA 4100 WITH TILT TABLE OPTION (K033244)Ge Medical Systems, Inc.2003-10-16
GE 1.5T 8 CHANNEL TORSO COIL (K031209)Ge Medical Systems, Inc.2003-05-23
CT COLONOGRAPHY (K023943)Ge Medical Systems, Inc.2003-05-06