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

MID LABS TWIN ILLUMINATOR

K Number: K932131 · Decision Apr 1, 1994
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
48
Applicant Total
22
Review Days
333

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Basic Information

Device Name
MID LABS TWIN ILLUMINATOR
K Number
K932131
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.4350
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medical Instrument Development Laboratories, Inc.
Date Received
May 3, 1993
Decision Date
April 1, 1994
Product Code
EQH
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EQH Source, Carrier, Fiberoptic Light

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Other Clearances by Medical Instrument Development Laboratories, Inc.

K Number Device Name
K102222 ULTIMATE VIT ENHAMCER (UVE)
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K992943 VIT ENHANCER
K971067 DIGI-INJECTOR
K950287 UNIVIT PROBE
K934600 MICRODRIVE
K932669 SUPRA-VIT(TM)
K924222 MID LABS, INC. VIT MATE
K851610 COMBINED MVS SYSTEMS
K851009 INFUSION SLEEVE - OPHTHALMIC
Search all 22 clearances from Medical Instrument Development Laboratories, Inc. →