FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DISPOSABLE HAND HELD NEBULIZER
K Number: K800562
·
Decision Mar 25, 1980
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
507
Applicant Total
17
Review Days
13
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Basic Information
- Device Name
- DISPOSABLE HAND HELD NEBULIZER
- K Number
- K800562
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5630
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Intec Medical, Inc.
- Date Received
- March 12, 1980
- Decision Date
- March 25, 1980
- Product Code
- CAF
- 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 |
|---|---|---|---|
| CAF | Nebulizer (Direct Patient Interface) | FDA class 2 | Anesthesiology |
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|---|---|---|---|
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| K900710 | INTERFLO MEDICAL MODEL F-1 THERMODILUTION CATHETER | Oct 19, 1990 | Substantially Equivalent |
| K903840 | GIANT LUMEN SAFETIP SERIES: ENDOMYOCARDIAL BIOPSY | Oct 16, 1990 | Substantially Equivalent |
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| K900998 | INTERVENTIONAL MEDICAL Y ADAPTER W/ADJUST. VALVE | Aug 14, 1990 | Substantially Equivalent |
| K901247 | TRI ADAPTER W/ADJUSTABLE HEMOSTASIS VALVES | Jul 31, 1990 | Substantially Equivalent |
| K894925 | AMCATH URETERAL DILATORS MODELS 7100,7110,7120 | Dec 13, 1989 | Substantially Equivalent |
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