SEIRIN SPINEX INTRADERMAL ACUPUNCTURE NEEDLES— 510(k) K963769

Substantially Equivalent

Seirin-America, Inc.

FDA 510(k) clearance K963769 for SEIRIN SPINEX INTRADERMAL ACUPUNCTURE NEEDLES, Substantially Equivalent on 1996-10-16. Applicant: Seirin-America, Inc..

Clearance details

Applicant: Seirin-America, Inc.
Product code: Code MQX
Advisory panel: General Hospital
Date received: 1996-09-19
Decision date: 1996-10-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Weymouth, MA, US

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