FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
37-701-1 PATIENT DOASE MONITOR WITH DETECTORS
K Number: K860469
·
Decision Apr 16, 1986
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
2
Applicant Total
40
Review Days
69
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Basic Information
- Device Name
- 37-701-1 PATIENT DOASE MONITOR WITH DETECTORS
- K Number
- K860469
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.5900
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- Victoreen, Inc.
- Date Received
- February 6, 1986
- Decision Date
- April 16, 1986
- Product Code
- KPZ
- 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 |
|---|---|---|---|
| KPZ | Generator, High Voltage, X-Ray, Therapeutic | FDA class 2 | Radiology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (KPZ), ordered by most recent decision date.
View allOther Clearances by Victoreen, Inc.
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| K974112 | VACUDAP, MODEL 2000, 2001 | Jan 29, 1998 | Substantially Equivalent |
| K973960 | MODEL 37-185 | Jan 14, 1998 | Substantially Equivalent |
| K964952 | VERIDOSE V (FIVE), MODEL NUMBER 37-705 | Jul 21, 1997 | Substantially Equivalent |
| K964785 | VERIDOSE DIODES | Jun 13, 1997 | Substantially Equivalent |
| K971382 | PRONE BREAST POSITIONING BOARD, MODEL #37-018 | Jun 6, 1997 | Substantially Equivalent |
| K952233 | CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628 | Jun 16, 1995 | Substantially Equivalent |
| K940660 | MODEL 37-720 DUAL DIODE DOSIMETRY SYSTEM | Dec 9, 1994 | Substantially Equivalent |
| K935435 | NUCLEAR ASSOC 37-08 SER, RAYCAST HP RADIO IMMOB SYST | Jul 29, 1994 | Substantially Equivalent |
| K941931 | DIAGNOSTIC X-RAY PATIENT EXPOSURE INDICATOR | May 26, 1994 | Substantially Equivalent |