FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
TALLEY MICRO SYSTEM/TALLEY RIPPLEBED
K Number: K914775
·
Decision Apr 10, 1992
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
101
Applicant Total
6
Review Days
170
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Basic Information
- Device Name
- TALLEY MICRO SYSTEM/TALLEY RIPPLEBED
- K Number
- K914775
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5550
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Talley Group, Ltd.
- Date Received
- October 23, 1991
- Decision Date
- April 10, 1992
- Product Code
- FNM
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| FNM | Mattress, Air Flotation, Alternating Pressure | FDA class 2 | General Hospital |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (FNM), ordered by most recent decision date.
PRESSURE GUARD SITE SELECT (A)
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MIGHTY AIR
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PHYSIO/1000
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SIMPULSE
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SUPER AIR 9000 ALTERNATING AIR FLOATATION MATTRESS SYSTEM
FDA 510(k)
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Other Clearances by Talley Group, Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K151263 | Venturi Gauze Wound Care Sets with Portal Drain | Feb 19, 2016 | Substantially Equivalent |
| K143004 | VENTURI MiNO TG600/14 | Jan 5, 2016 | Substantially Equivalent |
| K914774 | MULTIPULSE SEQUENTIAL COMPRESSION UNIT | Feb 11, 1992 | Substantially Equivalent |
| K914780 | TALLEY SD.500 SKIN PRESSURE EVALUATOR | Dec 19, 1991 | Substantially Equivalent |
| K914776 | OXFORD PRESSURE MONITOR/TALLEY PRESSURE MONITOR | Dec 19, 1991 | Substantially Equivalent |