FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
CANNULAS, DYNACOR'S NASAL OXYGEN
K Number: K790056
·
Decision Feb 5, 1979
Classifications
1
FEI Numbers
263
Registration Numbers
263
Same Product Code
41
Applicant Total
238
Review Days
27
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Basic Information
- Device Name
- CANNULAS, DYNACOR'S NASAL OXYGEN
- K Number
- K790056
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 868.5340
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Medline Industries, Inc.
- Date Received
- January 9, 1979
- Decision Date
- February 5, 1979
- Product Code
- CAT
- 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 |
|---|---|---|---|
| CAT | Cannula, Nasal, Oxygen | FDA class 1 | Anesthesiology |
Similar 510(k) Clearances
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