FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
VANGUARD SERIES GAS REGULATORS
K Number: K942751
·
Decision Feb 9, 1995
Classifications
1
FEI Numbers
111
Registration Numbers
112
Same Product Code
54
Applicant Total
111
Review Days
244
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Basic Information
- Device Name
- VANGUARD SERIES GAS REGULATORS
- K Number
- K942751
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 868.2700
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Buckman Co., Inc.
- Date Received
- June 10, 1994
- Decision Date
- February 9, 1995
- Product Code
- CAN
- 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 |
|---|---|---|---|
| CAN | Regulator, Pressure, Gas Cylinder | FDA class 1 | Anesthesiology |
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