FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ACI SILICATH THORACIC CATHETER
K Number: K942335
·
Decision Aug 9, 1994
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
76
Applicant Total
1
Review Days
85
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Basic Information
- Device Name
- ACI SILICATH THORACIC CATHETER
- K Number
- K942335
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4200
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- American Catheter
- Date Received
- May 16, 1994
- Decision Date
- August 9, 1994
- Product Code
- GBX
- Advisory Committee
- General, Plastic Surgery
- 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 |
|---|---|---|---|
| GBX | Catheter, Irrigation | FDA class 1 | General, Plastic Surgery |
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