FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
CARIE MED-TECH MODEL 210 RAINOUT DRAINAGE SYSTEM
K Number: K932722
·
Decision Aug 6, 1993
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
21
Applicant Total
1
Review Days
63
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Basic Information
- Device Name
- CARIE MED-TECH MODEL 210 RAINOUT DRAINAGE SYSTEM
- K Number
- K932722
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 868.5995
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Carie Med-Tech Services, Inc.
- Date Received
- June 4, 1993
- Decision Date
- August 6, 1993
- 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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