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FDA 510(k), K123710, UNITOX BOTOX SYRINGE
FDA 510(k), K123710, UNITOX BOTOX SYRINGE
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$149.00 USD
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510(K) Number: K123710
Device Name: UNITOX BOTOX SYRINGE
Manufacturer: BIO-MED USA INC
Device Classification Name: syringe, piston
Regulation Number: 880.5860
Classification Product Code: FMF
Date Received: 12/04/2012
Decision Date: 05/09/2013
Regulation Medical Specialty: General Hospital
Device Name: UNITOX BOTOX SYRINGE
Manufacturer: BIO-MED USA INC
Device Classification Name: syringe, piston
Regulation Number: 880.5860
Classification Product Code: FMF
Date Received: 12/04/2012
Decision Date: 05/09/2013
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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