FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
VACUUM SUCTION FILTER
K Number: K812139
·
Decision Aug 20, 1981
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
47
Applicant Total
3
Review Days
23
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Basic Information
- Device Name
- VACUUM SUCTION FILTER
- K Number
- K812139
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.6740
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- K & G Healthcare Ind., Inc.
- Date Received
- July 28, 1981
- Decision Date
- August 20, 1981
- Product Code
- KDQ
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| KDQ | Bottle, Collection, Vacuum | FDA class 2 | General Hospital |
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