Seirin-America, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SEIRIN PYONEX ACUPUNCTURE NEEDLES, SEIRIN JR ACUPUNCTURE NEEDLES
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Seirin-America, Inc. General Hospital ✕
4 devices
Cleared
Feb 10, 1997
SEIRIN PYONEX ACUPUNCTURE NEEDLES
General Hospital
19d
Cleared
Feb 10, 1997
SEIRIN JR ACUPUNCTURE NEEDLES
General Hospital
18d
Cleared
Oct 16, 1996
SEIRIN SPINEX INTRADERMAL ACUPUNCTURE NEEDLES
General Hospital
27d
Cleared
Aug 16, 1996
SEIRIN ACUPUNCTURE NEEDLES
General Hospital
29d