FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
GX-MOBILE X-RAY UNIT
K Number: K873982
·
Decision Oct 30, 1987
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
235
Applicant Total
14
Review Days
30
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Basic Information
- Device Name
- GX-MOBILE X-RAY UNIT
- K Number
- K873982
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1720
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- Gendex Corp.
- Date Received
- September 30, 1987
- Decision Date
- October 30, 1987
- Product Code
- IZL
- Advisory Committee
- Radiology
- Review Advisory Committee
- RA
- 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 |
|---|---|---|---|
| IZL | System, X-Ray, Mobile | FDA class 2 | Radiology |
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Other Clearances by Gendex Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K952598 | GX-PAN PANORAMIC DENTAL X-RAY SYSTEM | Jun 29, 1995 | Substantially Equivalent |
| K945682 | PROCESSOR, RADIOGRAPHIC-FILM, AUTOMATIC, DENTAL | Feb 9, 1995 | Substantially Equivalent |
| K935046 | GX-770 X-RAY CONTROL, MODEL 46-404600G4 | Feb 18, 1994 | Substantially Equivalent |
| K925094 | VISUALIX RADIOGRAPHIC IMAGE DETECTING AND PROCESS | Sep 29, 1993 | Substantially Equivalent |
| K931001 | ORALIX DC | Sep 14, 1993 | Substantially Equivalent |
| K932675 | GXP DENTAL X-RAY PROCESSOR | Jul 26, 1993 | Substantially Equivalent |
| K922165 | ATC725, ATC525, AND AP300 | Jul 27, 1992 | Substantially Equivalent |
| K920189 | GX-C CEPHALOMETER | Apr 28, 1992 | Substantially Equivalent |
| K894188 | GX-ELEVATOR | Oct 3, 1989 | Substantially Equivalent |
| K890083 | GX-2000 STATIONARY X-RAY GENERATOR | Mar 31, 1989 | Substantially Equivalent |