FDA 510(k), K980027, PEREGRINE SHIELDED DIFFUSION PROBE

FDA 510(k), K980027, PEREGRINE SHIELDED DIFFUSION PROBE

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510(K) Number: K980027
Device Name: PEREGRINE SHIELDED 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: 57
Fully redacted pages: 5
Content pages: 52

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