FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ENDO-SECURE
K Number: K840844
·
Decision Mar 16, 1984
Classifications
1
FEI Numbers
72
Registration Numbers
72
Same Product Code
18
Applicant Total
1
Review Days
21
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Basic Information
- Device Name
- ENDO-SECURE
- K Number
- K840844
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 868.5280
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Exidyne, Inc.
- Date Received
- February 24, 1984
- Decision Date
- March 16, 1984
- Product Code
- JAY
- 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 |
|---|---|---|---|
| JAY | Support, Breathing Tube | FDA class 1 | Anesthesiology |
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