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

CHIROFLEX LENS MICROSERT

K Number: K903574 · Decision Sep 17, 1990
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
38
Applicant Total
10
Review Days
40

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Basic Information

Device Name
CHIROFLEX LENS MICROSERT
K Number
K903574
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4300
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Chiron Ophthalmics
Date Received
August 8, 1990
Decision Date
September 17, 1990
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KYB), ordered by most recent decision date.

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Other Clearances by Chiron Ophthalmics

K Number Device Name
K915861 MEDILENS-CS CORNEAL SHIELD
K914311 CHIROFLEX II LENS MICROSERT(TM)
K905825 COLLAGEN SHIELD, VARIOUS MODELS
K903575 CHIROFLEX FORCEPS
K901880 MEDILENS(TM) CORNEAL SHIELD
K894162 OPTISOL
K885015 COI 72 HR COLLAGEN SHIELD
K885016 COI 24 HR COLLAGEN SHIELD
K882762 COLLAGEN SHIELD