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

STORZ MILLENNIUM MICROSURGICL SYSTEM HIGH SPEED VITRECTOMY SYSTEM

K Number: K980488 · Decision Mar 23, 1998
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
148
Applicant Total
101
Review Days
42

Basic Information

Device Name
STORZ MILLENNIUM MICROSURGICL SYSTEM HIGH SPEED VITRECTOMY SYSTEM
K Number
K980488
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4150
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
STORZ INSTRUMENT CO.
Date Received
February 9, 1998
Decision Date
March 23, 1998
Product Code
HQE
Advisory Committee
Ophthalmic
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
HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered

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