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FDA 510(k), K980025, PEREGRINE TAPERED DIFFUSION PROBE
FDA 510(k), K980025, PEREGRINE TAPERED DIFFUSION PROBE
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510(K) Number: K980025
Device Name: PEREGRINE TAPERED DIFFUSION PROBE
Manufacturer: PEREGRINE SURGICAL LTD.
Device Classification Name: endoilluminator
Regulation Number: 876.1500
Classification Product Code: MPA
Date Received: 01/05/1998
Decision Date: 03/31/1998
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: PEREGRINE TAPERED DIFFUSION PROBE
Manufacturer: PEREGRINE SURGICAL LTD.
Device Classification Name: endoilluminator
Regulation Number: 876.1500
Classification Product Code: MPA
Date Received: 01/05/1998
Decision Date: 03/31/1998
Regulation Medical Specialty: Gastroenterology/Urology
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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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