FDA 510(k) Unknown 🇺🇸 United States

OBSTETRICAL KIT

K Number: K863504 · Decision Oct 22, 1986
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
4
Review Days
43

Basic Information

Device Name
OBSTETRICAL KIT
K Number
K863504
Clearance Type
Traditional
Decision
Unknown
Applicant
DYNA-MED
Date Received
September 9, 1986
Decision Date
October 22, 1986
Advisory Committee
Unknown
Review Advisory Committee
OB
Third Party
N

Other Clearances by DYNA-MED

K Number Device Name
K884578 POLARIX 2 AND POLARIX 2E
K884340 AMX-110, AMX-II AND AMX-III
K760258 BITE STICK, DYNA