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

LASAG MICRORUPTOR 2 ND:YAG OPHTH. LASER SYSTEM

K Number: K885164 · Decision Jan 10, 1989
Classifications
1
FEI Numbers
60
Registration Numbers
61
Same Product Code
179
Applicant Total
34
Review Days
28

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Basic Information

Device Name
LASAG MICRORUPTOR 2 ND:YAG OPHTH. LASER SYSTEM
K Number
K885164
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4390
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Chiron Vision Corp.
Date Received
December 13, 1988
Decision Date
January 10, 1989
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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K941550 AUTOMATIC CORNEAL SHAPER SURGICAL INSTRUMENT
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