Atlas FDA

SSD-725 ULTRASOUND SECTOR SCANNER

FDA 510(k) clearance K870607 · decided 1987-08-10

Clearance details

K-number
K870607
Device name
SSD-725 ULTRASOUND SECTOR SCANNER
Applicant
Ge Medical Systems Information Technologies
Decision
Substantially Equivalent
Date received
1987-02-11
Decision date
1987-08-10
Days to decision
180 days
Clearance type
Traditional
Product code
JOP
Device class
2
Regulation number
870.2880
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Wallingford, CT, US
Third-party review
No
Expedited review
No

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FALCON (K111416)Viasonix , Ltd.2011-07-15
STUDIODOP VICORDER (K071730)Skidmore Medical, Limited2007-12-20
ECHOFLOW PORTABLE DOPPLER BLOOD FLOW MEASUREMENT SYSTEM; MODEL PEF-1 (K010482)Echocath, Inc.2001-03-20
NICOLET VASOGUARD (K002766)Nicolet Biomedical2000-11-30
ECHOFLOW DOPPLER BLOOD VELOCITY METER (K990642)Echocath, Inc.1999-09-16
SPECTRADOP (K925078)Bennett and Assoc., Inc.1995-07-17
REUSABLE CW DOPPLER PROBES: MODELS P8M05S8A, P8M05N5A, & LCW-8 (K934638)Koven Technology, Inc.1994-05-13

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
COROMETRICS MODEL 120 F-SERIES MATERNAL/FETAL MONITOR WITH INTERGRATED FETAL OXYGEN SATURATION MONITORING (P000016/S002)Ge Medical Systems Information Technologies2003-10-15
COROMETRICS MODEL 120 SERIES MATERNAL/FETAL MONITOR W/INTEGRATED FETAL PULSE OXIMETRY (P000016/S001)Ge Medical Systems Information Technologies2001-11-09
COROMETRICS 120F SERIES MATERNAL/FETAL MONITOR (P000016)Ge Medical Systems Information Technologies2001-02-09
MODEL 515 NEONATAL MONIOTR (P840037/S001)Ge Medical Systems Information Technologies1986-11-19