FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Model BT-220L and BT-220C

K Number: K142799 · Decision Jul 9, 2015
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
213
Applicant Total
11
Review Days
283

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Model BT-220L and BT-220C
K Number
K142799
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.2740
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bistos Co., Ltd.
Date Received
September 29, 2014
Decision Date
July 9, 2015
Product Code
HGM
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HGM System, Monitoring, Perinatal

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HGM), ordered by most recent decision date.

View all

Other Clearances by Bistos Co., Ltd.

K Number Device Name
K251512 Hi bebe super (BT-150B)
K232991 BT-1000
K210289 Infant Phototherapy Equipment
K200675 Hi bebe super (Models BT-150S and BT-150L)
K160274 Hi bebe plus
K132543 INFANT INCUBATOR
K121267 BT-200V VASCULAR DOPPLER
K103545 BT-350
K100885 FETAL MONITOR MODEL: BT-200T
K052190 FETAL MONITOR, MODELS BT-300 AND BT-200
Search all 11 clearances from Bistos Co., Ltd. →