FDA 510(k)
FDA class 1
Unknown
🇺🇸 United States
VACVENT
K Number: K931873
·
Decision Dec 30, 1993
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
57
Applicant Total
1
Review Days
260
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Basic Information
- Device Name
- VACVENT
- K Number
- K931873
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 868.1100
- Medical Specialty
- Anesthesiology
- Decision
- Unknown
- Statement or Summary
- Statement
- Applicant
- Steven Frank Mercereau
- Date Received
- April 14, 1993
- Decision Date
- December 30, 1993
- 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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