FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
COMBINED MVS SYSTEMS
K Number: K851610
·
Decision Jul 22, 1985
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
148
Applicant Total
22
Review Days
98
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Basic Information
- Device Name
- COMBINED MVS SYSTEMS
- K Number
- K851610
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 886.4150
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Applicant
- Medical Instrument Development Laboratories, Inc.
- Date Received
- April 15, 1985
- Decision Date
- July 22, 1985
- Product Code
- HQE
- 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 | Device Class | Medical Specialty |
|---|---|---|---|
| HQE | Instrument, Vitreous Aspiration And Cutting, Ac-Powered | FDA class 2 | Ophthalmic |
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| 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 |
| K932131 | MID LABS TWIN ILLUMINATOR | Apr 1, 1994 | Substantially Equivalent |
| K924222 | MID LABS, INC. VIT MATE | Jan 27, 1993 | Substantially Equivalent |
| K851009 | INFUSION SLEEVE - OPHTHALMIC | Apr 3, 1985 | Substantially Equivalent |