FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
MODIFIED NOFLO I
K Number: K871262
·
Decision Jul 21, 1987
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
8
Applicant Total
4
Review Days
112
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Basic Information
- Device Name
- MODIFIED NOFLO I
- K Number
- K871262
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 868.2300
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Design Technologies, Inc.
- Date Received
- March 31, 1987
- Decision Date
- July 21, 1987
- Product Code
- CCN
- 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 |
|---|---|---|---|
| CCN | Flowmeter, Nonback-Pressure Compensated, Bourdon Gauge | FDA class 1 | Anesthesiology |
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