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 | Device Class | Medical Specialty |
|---|---|---|---|
| EQH | Source, Carrier, Fiberoptic Light | FDA class 1 | Ear, Nose, Throat |
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Other Clearances by Medical Instrument Development Laboratories, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K102222 | ULTIMATE VIT ENHAMCER (UVE) | Apr 8, 2011 | Substantially Equivalent |
| K020911 | MID LABS AUTONOMOUS VIT ENHANCER (AVE) | Apr 29, 2002 | Substantially Equivalent |
| K992943 | VIT ENHANCER | Dec 10, 1999 | Substantially Equivalent |
| K971067 | DIGI-INJECTOR | Sep 19, 1997 | Substantially Equivalent |
| K950287 | UNIVIT PROBE | Apr 10, 1995 | Substantially Equivalent |
| K934600 | MICRODRIVE | Jul 27, 1994 | Substantially Equivalent |
| K932669 | SUPRA-VIT(TM) | Jun 3, 1994 | Substantially Equivalent |
| K924222 | MID LABS, INC. VIT MATE | Jan 27, 1993 | Substantially Equivalent |
| K851610 | COMBINED MVS SYSTEMS | Jul 22, 1985 | Substantially Equivalent |
| K851009 | INFUSION SLEEVE - OPHTHALMIC | Apr 3, 1985 | Substantially Equivalent |