FDA 510(k), K980025, PEREGRINE TAPERED DIFFUSION PROBE

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

Total pages: 73
Fully redacted pages: 4
Content pages: 69