FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ABDOMINAL/VASCULAR RETRACTOR-SPLIT WISHBONE 163000
K Number: K874243
·
Decision Nov 13, 1987
Classifications
1
FEI Numbers
656
Registration Numbers
656
Same Product Code
99
Applicant Total
39
Review Days
28
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Basic Information
- Device Name
- ABDOMINAL/VASCULAR RETRACTOR-SPLIT WISHBONE 163000
- K Number
- K874243
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4800
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Pilling Co.
- Date Received
- October 16, 1987
- Decision Date
- November 13, 1987
- Product Code
- GAD
- 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 |
|---|---|---|---|
| GAD | Retractor | FDA class 1 | General, Plastic Surgery |
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| K914015 | CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP | Nov 21, 1991 | Substantially Equivalent |
| K911099 | MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE | Jun 25, 1991 | Substantially Equivalent |
| K911100 | MEHIGAN-PILLING PHLEBETOME TM | Jun 21, 1991 | Substantially Equivalent |
| K904507 | PILLING BRUSH VALVULOTOME | Mar 1, 1991 | Substantially Equivalent |
| K884946 | JEHLE CORONARY PERFUSION CATHETERS | Feb 6, 1989 | Substantially Equivalent |
| K882930 | LASER LARYNGOSCOPE DEDO ARTICULA. & FEDER DEDO EX | Aug 16, 1988 | Substantially Equivalent |