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

ML UNIVERSAL TUBING

K Number: K983448 · Decision Dec 18, 1998
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
4
Applicant Total
12
Review Days
79

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Basic Information

Device Name
ML UNIVERSAL TUBING
K Number
K983448
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4150
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Med-Logics, Inc.
Date Received
September 30, 1998
Decision Date
December 18, 1998
Product Code
MSR
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
MSR Tubing, Replacement, Phacofragmentation Unit

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MSR), 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
K022982 MED-LOGICS MICROKERATOME BLADE, MODEL 7050CLB
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
K981071 ML MICROKERATOME
K972522 ML-DISPOSABLE PAK
K971173 ML DISPOSABLE ALK TUBING
Search all 12 clearances from Med-Logics, Inc. →