FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ICE CONTAINER I.C.E.
K Number: K792182
·
Decision Nov 15, 1979
Classifications
1
FEI Numbers
467
Registration Numbers
468
Same Product Code
26
Applicant Total
27
Review Days
17
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Basic Information
- Device Name
- ICE CONTAINER I.C.E.
- K Number
- K792182
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 890.5700
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Applicant
- Delta Medical Industries
- Date Received
- October 29, 1979
- Decision Date
- November 15, 1979
- Product Code
- IME
- Advisory Committee
- Physical Medicine
- Review Advisory Committee
- PM
- 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 |
|---|---|---|---|
| IME | Pack, Hot Or Cold, Reusable | FDA class 1 | Physical Medicine |
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|---|---|---|---|
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| K832470 | INFUSION PUMP | Feb 28, 1984 | Substantially Equivalent |
| K830389 | ACCU-RYNGE PUMP SP-250 | Sep 12, 1983 | Substantially Equivalent |
| K831750 | PM-3 | Jul 26, 1983 | Substantially Equivalent |
| K822761 | DELIVERY TUBE SET #2226 | Sep 30, 1982 | Substantially Equivalent |
| K820912 | PMS-2 PRESSURE MONITOR SEPARATOR | May 18, 1982 | Substantially Equivalent |
| K820482 | ACCU-RYNGE INSULIN PUMP #SP-250 | Mar 26, 1982 | Substantially Equivalent |
| K810068 | PEDIATRIC ARTERIAL BLOOD FILTER | Jan 22, 1981 | Substantially Equivalent |
| K802755 | ARTERIAL BLOOD FILTER BF-37 | Jan 7, 1981 | Substantially Equivalent |