FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
REVJET TURBO
K Number: K060842
·
Decision Jun 21, 2006
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
507
Applicant Total
16
Review Days
85
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Basic Information
- Device Name
- REVJET TURBO
- K Number
- K060842
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5630
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Promedic, Inc.
- Date Received
- March 28, 2006
- Decision Date
- June 21, 2006
- Product Code
- CAF
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- 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 |
|---|---|---|---|
| CAF | Nebulizer (Direct Patient Interface) | FDA class 2 | Anesthesiology |
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|---|---|---|---|
| K131889 | EUM 100PRO | Apr 23, 2014 | Substantially Equivalent |
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| K060497 | BABYAIR | Jul 11, 2006 | Substantially Equivalent |
| K052903 | PEDIATRIC FEEDING TUBE | Nov 9, 2005 | Substantially Equivalent |
| K031409 | URINARY CATHETERS | Jun 17, 2003 | Substantially Equivalent |
| K024190 | FENESTRATED INFUSION CATHETER | Mar 17, 2003 | Substantially Equivalent |
| K023579 | GAS SAMPLING LINES | Jan 28, 2003 | Substantially Equivalent |
| K020005 | INFANT FEEDING TUBES | Jul 16, 2002 | Substantially Equivalent |
| K970102 | FILTER | Jun 24, 1997 | Substantially Equivalent |