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

HESSBURG GLIDE UNTRAOCULAR LENS GUIDES

K Number: K852529 · Decision Sep 24, 1985
Classifications
1
FEI Numbers
60
Registration Numbers
61
Same Product Code
179
Applicant Total
49
Review Days
102

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Basic Information

Device Name
HESSBURG GLIDE UNTRAOCULAR LENS GUIDES
K Number
K852529
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4390
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Visitec Co.
Date Received
June 14, 1985
Decision Date
September 24, 1985
Product Code
HQF
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
HQF Laser, Ophthalmic

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