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

ML EYE SPEAR, MODEL ML 27 ES

K Number: K002279 · Decision Aug 18, 2000
Classifications
1
FEI Numbers
77
Registration Numbers
78
Same Product Code
46
Applicant Total
12
Review Days
23

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Basic Information

Device Name
ML EYE SPEAR, MODEL ML 27 ES
K Number
K002279
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4790
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Med-Logics, Inc.
Date Received
July 26, 2000
Decision Date
August 18, 2000
Product Code
HOZ
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
HOZ Sponge, Ophthalmic

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Other Clearances by Med-Logics, Inc.

K Number Device Name
K033293 MED-LOGICS, MODEL ML7090
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K022716 MED-LOGICS MICROKERATOME BLADE, MODEL 7020CLB
K010872 ML BLADE, MODEL ML7030
K010353 MED-LOGICS DISPOSABLE ALK TUBING
K002515 MEDLOGICS ML 4000, MODEL 4000
K983448 ML UNIVERSAL TUBING
K981071 ML MICROKERATOME
K972522 ML-DISPOSABLE PAK
K971173 ML DISPOSABLE ALK TUBING
Search all 12 clearances from Med-Logics, Inc. →