FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
NIDEK MODEL NT-1000
K Number: K913189
·
Decision Oct 15, 1991
Classifications
1
FEI Numbers
36
Registration Numbers
37
Same Product Code
57
Applicant Total
77
Review Days
89
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Basic Information
- Device Name
- NIDEK MODEL NT-1000
- K Number
- K913189
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 886.1930
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Nidek, Inc.
- Date Received
- July 18, 1991
- Decision Date
- October 15, 1991
- Product Code
- HKX
- 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 |
|---|---|---|---|
| HKX | Tonometer, Ac-Powered | FDA class 2 | Ophthalmic |
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|---|---|---|---|
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| K031733 | NON-CONTACT TONOMETER, MODEL NT-4000 | Dec 4, 2003 | Substantially Equivalent |
| K032085 | GREEN LASER PHOTOCOAGULATOR MODEL GYC-1000 | Oct 3, 2003 | Substantially Equivalent |
| K013694 | NIDEK ADVANCED VISION INFORMATION SYSTEM (NAVIS) | Nov 19, 2002 | Substantially Equivalent |
| K020876 | ECHOSCAN, MODEL US-1800 | May 3, 2002 | Substantially Equivalent |
| K014274 | NON-MYDRIATIC FUNDUS CAMERA, MODEL NM-1000 | Apr 17, 2002 | Substantially Equivalent |
| K013760 | DC-3300 LASER DIODE PHOTOCOAGULATOR | Feb 11, 2002 | Substantially Equivalent |
| K013864 | MODIFICATION TO EPI-STAR SURGICAL LASER SYSTEM, M0DEL DS-60 | Feb 8, 2002 | Substantially Equivalent |
| K990119 | EPI-STAR SURGICAL LASER SYSTER | Jul 27, 2000 | Substantially Equivalent |