FDA 510(k)
FDA unclassified
Substantially Equivalent
🇩🇰 Denmark
NYDIAG 200
K Number: K102364
·
Decision Dec 23, 2010
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
21
Applicant Total
17
Review Days
125
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Basic Information
- Device Name
- NYDIAG 200
- K Number
- K102364
- Device Class
- FDA unclassified
- Clearance Type
- Traditional
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Interacoustics A/S
- Date Received
- August 20, 2010
- Decision Date
- December 23, 2010
- Product Code
- LXV
- Advisory Committee
- Unknown
- 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 |
|---|---|---|---|
| LXV | Apparatus, Vestibular Analysis | FDA unclassified | Unknown |
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|---|---|---|---|
| K200534 | VisualEyes | Aug 12, 2020 | Substantially Equivalent |
| K200529 | Orion | Aug 12, 2020 | Substantially Equivalent |
| K192652 | TRV | May 27, 2020 | Substantially Equivalent |
| K191372 | Lyra | Jul 15, 2019 | Substantially Equivalent |
| K173567 | Sera | Feb 14, 2018 | Substantially Equivalent |
| K163149 | VisualEyes | Apr 26, 2017 | Substantially Equivalent |
| K162037 | Eclipse with VEMP | Mar 23, 2017 | Substantially Equivalent |
| K152112 | VisualEyes | Dec 29, 2015 | Substantially Equivalent |
| K151616 | AT235 | Jul 15, 2015 | Substantially Equivalent |
| K131681 | EYESEECAM VHIT | Sep 6, 2013 | Substantially Equivalent |