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

VIT ENHANCER

K Number: K992943 · Decision Dec 10, 1999
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
148
Applicant Total
22
Review Days
101

Basic Information

Device Name
VIT ENHANCER
K Number
K992943
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4150
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MEDICAL INSTRUMENT DEVELOPMENT LABORATORIES, INC.
Date Received
August 31, 1999
Decision Date
December 10, 1999
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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