FDA 510(k)
FDA unclassified
Substantially Equivalent
🇺🇸 United States
AQUACEL AG SURGICAL
K Number: K091034
·
Decision Dec 16, 2009
Classifications
1
FEI Numbers
384
Registration Numbers
385
Same Product Code
702
Applicant Total
7
Review Days
250
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Basic Information
- Device Name
- AQUACEL AG SURGICAL
- K Number
- K091034
- Device Class
- FDA unclassified
- Clearance Type
- Traditional
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Convatec
- Date Received
- April 10, 2009
- Decision Date
- December 16, 2009
- Product Code
- FRO
- Advisory Committee
- Unknown
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| FRO | Dressing, Wound, Drug | FDA unclassified | Unknown |
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|---|---|---|---|
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| K243228 | Flexi-Seal AIR (with ENFit Connector) | Mar 28, 2025 | Substantially Equivalent |
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| K162906 | Flexi-Seal PROTECT Fecal Management System | Mar 7, 2017 | Substantially Equivalent |
| K083785 | VITALA CONTINENCE CONTROL DEVICE | Apr 2, 2010 | Substantially Equivalent |
| K071763 | AMADEUS ADAPTIVE COMPRESSION THERAPY | Mar 7, 2008 | Substantially Equivalent |