FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
SAFETY DRAIN
K Number: K881790
·
Decision Jun 21, 1988
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
21
Applicant Total
26
Review Days
56
Basic Information
- Device Name
- SAFETY DRAIN
- K Number
- K881790
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 868.5995
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- BALLARD MEDICAL PRODUCTS
- Date Received
- April 26, 1988
- Decision Date
- June 21, 1988
- Product Code
- BYH
- 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 |
|---|---|---|---|
| BYH | Drain, Tee (Water Trap) | FDA class 1 | Anesthesiology |
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