SEIRIN PYONEX ACUPUNCTURE NEEDLES— 510(k) K970254

Substantially Equivalent

Seirin-America, Inc.

FDA 510(k) clearance K970254 for SEIRIN PYONEX ACUPUNCTURE NEEDLES, Substantially Equivalent on 1997-02-10. Applicant: Seirin-America, Inc..

Clearance details

Applicant: Seirin-America, Inc.
Product code: Code MQX
Advisory panel: General Hospital
Date received: 1997-01-22
Decision date: 1997-02-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Weymouth, MA, US

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