FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

PEREGRINE SHIELDED DIFFUSION PROBE

K Number: K980027 · Decision Mar 31, 1998
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
39
Applicant Total
19
Review Days
85

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Basic Information

Device Name
PEREGRINE SHIELDED DIFFUSION PROBE
K Number
K980027
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Peregrine Surgical , Ltd.
Date Received
January 5, 1998
Decision Date
March 31, 1998
Product Code
MPA
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
OP
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MPA Endoilluminator

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Other Clearances by Peregrine Surgical , Ltd.

K Number Device Name
K151604 23ga Chandelier Illuminator, 25ga Chandelier Illuminator
K132614 PEREGRINE CURVED ILLUMINATING LASER PROBE
K122997 23GA CURVED ILLUMINATING LASER PROBE
K122905 PEREGRINE 23GA CURVED LASER PROBE
K061024 PEREGRINE SOFT TIP ASPIRATING LASER PROBE, MODEL PD720.60
K031023 PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10
K024061 PEREGRINE STRAIGHT LASER PROBE, MODEL PD6000.00
K990518 PEREGRINE WET SET, MODEL PD400.00
K981907 V.F.I.-VISCOUS FLUID INFUSION TUBING SET
K980797 PEREGRINE FIBER OPTIC MULTI-FUNCTION MANIPULATOR
Search all 19 clearances from Peregrine Surgical , Ltd. →