FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SUCTION REGULATOR 7700 SERIES
K Number: K850200
·
Decision Mar 4, 1985
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
20
Applicant Total
37
Review Days
45
Basic Information
- Device Name
- SUCTION REGULATOR 7700 SERIES
- K Number
- K850200
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.6740
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- BOEHRINGER LABORATORIES
- Date Received
- January 18, 1985
- Decision Date
- March 4, 1985
- Product Code
- KDP
- 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 |
|---|---|---|---|
| KDP | Regulator, Vacuum | FDA class 2 | General Hospital |
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