FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PEEP/CPAP VALVE
K Number: K781332
·
Decision Oct 4, 1978
Classifications
1
FEI Numbers
71
Registration Numbers
72
Same Product Code
79
Applicant Total
22
Review Days
63
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Basic Information
- Device Name
- PEEP/CPAP VALVE
- K Number
- K781332
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5965
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Vickers America Medical Corp.
- Date Received
- August 2, 1978
- Decision Date
- October 4, 1978
- Product Code
- BYE
- 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 |
|---|---|---|---|
| BYE | Attachment, Breathing, Positive End Expiratory Pressure | FDA class 2 | Anesthesiology |
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| K813239 | OXYGENAIRE NURING INCUBATOR | Jan 28, 1982 | Substantially Equivalent |
| K813238 | NEOCARE BABY-CONTROLLED INCUBATOR | Jan 22, 1982 | Substantially Equivalent |
| K811865 | VMA PEDIATRIC APNEA MATTRESS | Jul 31, 1981 | Substantially Equivalent |
| K810792 | NEOCARE TEMPERATURE MONITOR | Apr 29, 1981 | Substantially Equivalent |
| K810067 | 140 NEOCARE AIR CONTROLLED INCUBATOR | Mar 11, 1981 | Substantially Equivalent |
| K810571 | NEOCARE OXYGEN MONITOR | Mar 11, 1981 | Substantially Equivalent |