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

PRISMA DISPOSABLE PUPIL CENTERING CANNULA

K Number: K875003 · Decision Apr 13, 1988
Classifications
1
FEI Numbers
234
Registration Numbers
235
Same Product Code
76
Applicant Total
64
Review Days
131

Basic Information

Device Name
PRISMA DISPOSABLE PUPIL CENTERING CANNULA
K Number
K875003
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4350
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
ADVANCED SURGICAL PRODUCTS, INC.
Date Received
December 4, 1987
Decision Date
April 13, 1988
Product Code
HMX
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
HMX Cannula, Ophthalmic

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