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

CANNULAS

K Number: K790243 · Decision Feb 12, 1979
Classifications
1
FEI Numbers
234
Registration Numbers
235
Same Product Code
76
Applicant Total
49
Review Days
45

Basic Information

Device Name
CANNULAS
K Number
K790243
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4350
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
VISITEC CO.
Date Received
December 29, 1978
Decision Date
February 12, 1979
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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