FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
TOMEY PE-400 PORTABLE ERG & VEP WITH OPTIONAL PS-4
K Number: K932571
·
Decision Aug 31, 1995
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
48
Applicant Total
9
Review Days
826
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Basic Information
- Device Name
- TOMEY PE-400 PORTABLE ERG & VEP WITH OPTIONAL PS-4
- K Number
- K932571
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.1890
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Tomey Corporation USA
- Date Received
- May 27, 1993
- Decision Date
- August 31, 1995
- Product Code
- GWE
- Advisory Committee
- Neurology
- Review Advisory Committee
- NE
- 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 |
|---|---|---|---|
| GWE | Stimulator, Photic, Evoked Response | FDA class 2 | Neurology |
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Other Clearances by Tomey Corporation USA
| K Number | Device Name | ||
|---|---|---|---|
| K971953 | CONFOSCAN | Aug 14, 1997 | Substantially Equivalent |
| K971685 | IMAGESCAPE DIGITAL RETINAL IMAGE SYSTEM | Jun 24, 1997 | Substantially Equivalent |
| K961805 | TOMEY DTL ELECTRODE | May 9, 1997 | Substantially Equivalent |
| K945959 | VIDEO VISION ANALYZER (VIVA), VRB 100 | Mar 1, 1995 | Substantially Equivalent |
| K944910 | TOMEY EM-1000 SPECULAR MICROSCOPE | Nov 22, 1994 | Substantially Equivalent |
| K924760 | TOMEY PROTON TONOMETER | Apr 5, 1993 | Substantially Equivalent |
| K921815 | TOMEY PE-300 PORTABLE ERG | Jul 15, 1992 | Substantially Equivalent |
| K912112 | PF-400,GF-300,IF-200,PG400,PG400C,AND ED-480 | Jun 17, 1991 | Substantially Equivalent |