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FDA 510(k), K052846, TEWA CJ-TYPE, PJ-TYPE, CB-TYPE AND PB-TYPE ACUPUNCTURE NEEDLES FOR SINGLE USE
FDA 510(k), K052846, TEWA CJ-TYPE, PJ-TYPE, CB-TYPE AND PB-TYPE ACUPUNCTURE NEEDLES FOR SINGLE USE
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510(K) Number: K052846
Device Name: TEWA CJ-TYPE, PJ-TYPE, CB-TYPE AND PB-TYPE ACUPUNCTURE NEEDLES FOR SINGLE USE
Manufacturer: MAANSHAN MEDICAL INSTRUMENTS CO., LTD.
Device Classification Name: needle, acupuncture, single use
Regulation Number: 880.5580
Classification Product Code: MQX
Date Received: 10/07/2005
Decision Date: 12/22/2005
Regulation Medical Specialty: General Hospital
Device Name: TEWA CJ-TYPE, PJ-TYPE, CB-TYPE AND PB-TYPE ACUPUNCTURE NEEDLES FOR SINGLE USE
Manufacturer: MAANSHAN MEDICAL INSTRUMENTS CO., LTD.
Device Classification Name: needle, acupuncture, single use
Regulation Number: 880.5580
Classification Product Code: MQX
Date Received: 10/07/2005
Decision Date: 12/22/2005
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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