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FDA 510(k), K021904, MAEDA SILVER ACUPUNCTURE NEEDLE
FDA 510(k), K021904, MAEDA SILVER ACUPUNCTURE NEEDLE
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510(K) Number: K021904
Device Name: MAEDA SILVER ACUPUNCTURE NEEDLE
Manufacturer: E.J. Smith
Device Classification Name: Needle, Acupuncture, Single Use
Regulation Number: MQX
Classification Product Code: KXA
Date Received: 06/10/2002
Decision Date: 08/14/2002
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: MAEDA SILVER ACUPUNCTURE NEEDLE
Manufacturer: E.J. Smith
Device Classification Name: Needle, Acupuncture, Single Use
Regulation Number: MQX
Classification Product Code: KXA
Date Received: 06/10/2002
Decision Date: 08/14/2002
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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