FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇱 Israel
LAB-SITE(R) SAFETY CANNULA
K Number: K933929
·
Decision Dec 7, 1993
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
68
Applicant Total
15
Review Days
119
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Basic Information
- Device Name
- LAB-SITE(R) SAFETY CANNULA
- K Number
- K933929
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5470
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Migada, Ltd.
- Date Received
- August 10, 1993
- Decision Date
- December 7, 1993
- Product Code
- CBF
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- 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 |
|---|---|---|---|
| CBF | Chamber, Hyperbaric | FDA class 2 | Anesthesiology |
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Other Clearances by Migada, Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K943095 | IV TRANSFER SPIKE | Sep 30, 1994 | Substantially Equivalent |
| K902881 | LAB-SITE SAFETY NEEDLE | Sep 26, 1990 | Substantially Equivalent |
| K870016 | ARTERIAL BLOOD GASSING MONITORING SYSTEM (ABG) | May 28, 1987 | Substantially Equivalent |
| K864453 | EMERGENCY & MILITARY INFUSION SYSTEM | Jan 20, 1987 | Substantially Equivalent |
| K863304 | PRESELECTED FLOW RATE I.V. SET | Dec 9, 1986 | Substantially Equivalent |
| K860952 | I.V. SET WITH AND WITHOUT AIR VENT | Aug 27, 1986 | Substantially Equivalent |
| K861275 | HIGH FLOW I.V. SET | Jun 2, 1986 | Substantially Equivalent |
| K860595 | TRANSFER SET | Apr 7, 1986 | Substantially Equivalent |
| K854365 | IV SETS WITH NO PHTHALATE PLASTICIZER COMPONENTS | Mar 24, 1986 | Substantially Equivalent |
| K860605 | FILTER SET 1) 1.2 MIC FILTER 2) 3.0 MIC FILTER | Mar 24, 1986 | Substantially Equivalent |