FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEM
K Number: K062302
·
Decision Oct 6, 2006
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
47
Applicant Total
1
Review Days
59
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEM
- K Number
- K062302
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.6740
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Millicore AB
- Date Received
- August 8, 2006
- Decision Date
- October 6, 2006
- 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 |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (KDQ), ordered by most recent decision date.
EXPRESS CHEST DRAIN
FDA 510(k)
FDA Class 2
·General Hospital
OCEAN CHEST DRAIN
FDA 510(k)
FDA Class 2
·General Hospital
ATRIUM MEDICAL CORPORATION EXPRESS CHEST DRAIN
FDA 510(k)
FDA Class 2
·General Hospital
PLEUR-EVAC SAHARA ADULT/PEDIATRIC CHEST DRAINAGE SYSTEM MODEL S-1100, S-1200, 2-2100, AND S-2200 WITH MODEL S-100 AUTOTR
FDA 510(k)
FDA Class 2
·General Hospital
ROCKET PLEURASEAL II CHEST DRAINAGE SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
MUCUS SPECIMEN TRAP
FDA 510(k)
FDA Class 2
·General Hospital