FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIED
K Number: K933232
·
Decision Mar 28, 1994
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
20
Applicant Total
38
Review Days
265
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Basic Information
- Device Name
- BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIED
- K Number
- K933232
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.6740
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Boehringer Laboratories
- Date Received
- July 6, 1993
- Decision Date
- March 28, 1994
- 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 |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (KDP), ordered by most recent decision date.
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OHMEDA CONTINUOUS SUCTION REGULATOR
FDA 510(k)
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