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

STORZ DISPOSABLE BIPOLAR PENCILS

K Number: K882802 · Decision Aug 17, 1988
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
65
Applicant Total
101
Review Days
41

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Basic Information

Device Name
STORZ DISPOSABLE BIPOLAR PENCILS
K Number
K882802
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4725
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Storz Instrument Co.
Date Received
July 7, 1988
Decision Date
August 17, 1988
Product Code
GXI
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
GXI Probe, Radiofrequency Lesion

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K960003 STORZ D7116 MICROVIT VITRECTOMY CUTTER EXTENSION
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