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

MED-LOGICS MICROKERATOME BLADE, MODEL 7050CLB

K Number: K022982 · Decision Nov 15, 2002
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
82
Applicant Total
12
Review Days
67

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Basic Information

Device Name
MED-LOGICS MICROKERATOME BLADE, MODEL 7050CLB
K Number
K022982
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4370
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Med-Logics, Inc.
Date Received
September 9, 2002
Decision Date
November 15, 2002
Product Code
HNO
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
HNO Keratome, Ac-Powered

Similar 510(k) Clearances

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

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Other Clearances by Med-Logics, Inc.

K Number Device Name
K033293 MED-LOGICS, MODEL ML7090
K022716 MED-LOGICS MICROKERATOME BLADE, MODEL 7020CLB
K010872 ML BLADE, MODEL ML7030
K010353 MED-LOGICS DISPOSABLE ALK TUBING
K002515 MEDLOGICS ML 4000, MODEL 4000
K002279 ML EYE SPEAR, MODEL ML 27 ES
K983448 ML UNIVERSAL TUBING
K981071 ML MICROKERATOME
K972522 ML-DISPOSABLE PAK
K971173 ML DISPOSABLE ALK TUBING
Search all 12 clearances from Med-Logics, Inc. →