FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

DISPOSABLE MICROSTAAR INJECTOR

K Number: K940593 · Decision Sep 19, 1994
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
38
Applicant Total
1
Review Days
222

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Basic Information

Device Name
DISPOSABLE MICROSTAAR INJECTOR
K Number
K940593
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4300
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Staar Sugical
Date Received
February 9, 1994
Decision Date
September 19, 1994
Product Code
KYB
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
KYB Lens, Guide, Intraocular

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