FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
DESERET ARTERIAL BLOOD SAMPLING KIT
K Number: K822248
·
Decision Oct 21, 1982
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
57
Applicant Total
50
Review Days
84
Basic Information
- Device Name
- DESERET ARTERIAL BLOOD SAMPLING KIT
- K Number
- K822248
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 868.1100
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- WARNER-LAMBERT CO.
- Date Received
- July 29, 1982
- Decision Date
- October 21, 1982
- Product Code
- CBT
- 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 |
|---|---|---|---|
| CBT | Arterial Blood Sampling Kit | FDA class 1 | Anesthesiology |
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