Medical Device Manufacturer · US , Weymouth , MA

Seirin-America, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1996

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Seirin-America, Inc. General Hospital ✕

4 devices

1-4 of 4

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