FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
OMNIMED I.V. SOLUTION ADMIN. SET
K Number: K853255
·
Decision Aug 23, 1985
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
12
Review Days
21
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Basic Information
- Device Name
- OMNIMED I.V. SOLUTION ADMIN. SET
- K Number
- K853255
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5440
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Omni Intl., Inc.
- Date Received
- August 2, 1985
- Decision Date
- August 23, 1985
- Product Code
- FPA
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| FPA | Set, Administration, Intravascular | FDA class 2 | General Hospital |
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Other Clearances by Omni Intl., Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K984066 | OMNIGRIP, LATEX SURGICAL GLOVE, POWDER-FREE WITH PROTEIN LABELING CLAIM | Jan 13, 1999 | Substantially Equivalent |
| K984064 | OMNIGRIP, LATEX SURGICAL GLOVE, POWDER FREE | Jan 8, 1999 | Substantially Equivalent |
| K851938 | OMNIMED SURGICAL GOWN | Jun 28, 1985 | Substantially Equivalent |
| K851654 | OMNIMED CLAMP | May 31, 1985 | Substantially Equivalent |
| K851734 | OMNIMED SUPERIOR TRANSDUCER PROTECTOR | May 23, 1985 | Substantially Equivalent |
| K850706 | F-SERIES IMPLANT | Apr 10, 1985 | Substantially Equivalent |
| K850112 | OMNIMED IV SOLUTION ADMINISTRATION SET | Feb 22, 1985 | Substantially Equivalent |
| K850066 | OMNIMED NASAL OXYGEN CANNULA | Jan 24, 1985 | Substantially Equivalent |
| K831147 | OMNIPROBE ELECTRICAL NERVE STIMULATOR | Jul 18, 1983 | Substantially Equivalent |
| K821523 | OMNI TENS | Jun 16, 1982 | Substantially Equivalent |