FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
JELCO & KVO CATHETER PLACEMENT UNIT
K Number: K791372
·
Decision Sep 12, 1979
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
13
Applicant Total
26
Review Days
50
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Basic Information
- Device Name
- JELCO & KVO CATHETER PLACEMENT UNIT
- K Number
- K791372
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4200
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Jelco Laboratories
- Date Received
- July 24, 1979
- Decision Date
- September 12, 1979
- Product Code
- JCY
- 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 |
|---|---|---|---|
| JCY | Catheter, Infusion | FDA class 1 | General, Plastic Surgery |
Similar 510(k) Clearances
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Other Clearances by Jelco Laboratories
| K Number | Device Name | ||
|---|---|---|---|
| K791918 | JELCO WINGED INTRAVASCULAR CATHETER | Oct 2, 1979 | Substantially Equivalent |
| K790967 | CATHETER METAL HUB/RADIOPAQUE | Jun 27, 1979 | Substantially Equivalent |
| K790968 | CATHETER METAL HUB/NONRADIOPAQUE | Jun 11, 1979 | Substantially Equivalent |
| K790471 | JELCO* DISC FILTER-0.2 MICRON | Apr 30, 1979 | Substantially Equivalent |
| K790186 | PROTECTIVSTABILIZER | Feb 26, 1979 | Substantially Equivalent |
| K790079 | NEEDLE, BLOOD COLLECTING | Feb 1, 1979 | Substantially Equivalent |
| K790107 | CATHETER TUBING MODIFICATION | Feb 1, 1979 | Substantially Equivalent |
| K781857 | TRAY, ARTERIAL BLOOD GAS SAMPLING | Dec 11, 1978 | Substantially Equivalent |
| K780896 | NEEDLES, DESIGN CHANGE, IV CATHETERS | Aug 23, 1978 | Substantially Equivalent |
| K780519 | FILTER TUBE | May 9, 1978 | Substantially Equivalent |