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

V.F.I.-VISCOUS FLUID INFUSION TUBING SET

K Number: K981907 · Decision Aug 4, 1998
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
18
Applicant Total
19
Review Days
64

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Basic Information

Device Name
V.F.I.-VISCOUS FLUID INFUSION TUBING SET
K Number
K981907
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Peregrine Surgical , Ltd.
Date Received
June 1, 1998
Decision Date
August 4, 1998
Product Code
MRH
Advisory Committee
General Hospital
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
MRH Pump, Infusion, Ophthalmic

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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
K980797 PEREGRINE FIBER OPTIC MULTI-FUNCTION MANIPULATOR
K980530 PEREGRINE FIBER OPTIC BIPOLAR STRAIGHT PICK AND ANGLED PICK, MODELS PD100.12 AND PD100.13
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