FDA 510(k)
FDA class 2
Substantially Equivalent for Some Indications
🇺🇸 United States
ALPHA TALKER
K Number: K935317
·
Decision Mar 28, 1994
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
580
Applicant Total
9
Review Days
144
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Basic Information
- Device Name
- ALPHA TALKER
- K Number
- K935317
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 890.3860
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent for Some Indications
- Applicant
- Prentke Romich Co.
- Date Received
- November 4, 1993
- Decision Date
- March 28, 1994
- Product Code
- ITI
- Advisory Committee
- Physical Medicine
- Review Advisory Committee
- PM
- 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 |
|---|---|---|---|
| ITI | Wheelchair, Powered | FDA class 2 | Physical Medicine |
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Other Clearances by Prentke Romich Co.
| K Number | Device Name | ||
|---|---|---|---|
| K961306 | DELTATALKER WITH INFRARED | Jun 27, 1996 | Substantially Equivalent |
| K944585 | SCANNING DIRECTOR | Feb 21, 1995 | Substantially Equivalent |
| K933207 | WALKERTALKER | Mar 28, 1994 | Substantially Equivalent for Some Indications |
| K925387 | LIBERATOR | Mar 29, 1993 | Substantially Equivalent |
| K925527 | LIGHT TALKER | Mar 22, 1993 | Substantially Equivalent |
| K914259 | TOUCH TALKER | Feb 27, 1992 | Substantially Equivalent |
| K902664 | HOSPITAL/HOME ENVIRONMENTAL CONTROL SYST/HECS-1 | Jul 25, 1990 | Substantially Equivalent |
| K902206 | CONTROL 1 ENVIRONMENTAL CONTROL | May 29, 1990 | Substantially Equivalent |