FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DRAKE WILLOCK REVERSE OSMOSIS WATER TREATMENT SYST
K Number: K894106
·
Decision Nov 8, 1989
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
116
Applicant Total
11
Review Days
152
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Basic Information
- Device Name
- DRAKE WILLOCK REVERSE OSMOSIS WATER TREATMENT SYST
- K Number
- K894106
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.5665
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Applicant
- Cd Medical, Inc.
- Date Received
- June 9, 1989
- Decision Date
- November 8, 1989
- Product Code
- FIP
- Advisory Committee
- Gastroenterology, Urology
- Review Advisory Committee
- GU
- 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 |
|---|---|---|---|
| FIP | Subsystem, Water Purification | FDA class 2 | Gastroenterology, Urology |
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Other Clearances by Cd Medical, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K925654 | CD HOME DIALYSERVICE HEMODIALYSIS TRAY | Mar 30, 1994 | Unknown |
| K910215 | DRAKE WILLOCK SYSTEM 1000 DIALYSATE DELIVERY SYST | Apr 9, 1991 | Substantially Equivalent |
| K901520 | WURTZ CHOLEY CLIP (TM) | Jun 26, 1990 | Substantially Equivalent |
| K884353 | ULTRX(TM) 850 ARTIFICIAL KIDNEY | Dec 8, 1988 | Substantially Equivalent |
| K880459 | 480 HIGH-FLOW ULTRAFILTRATION CONTROL DIALYSATE | Apr 13, 1988 | Substantially Equivalent |
| K873279 | 8810 PUMP-PUMP SINGLE NEEDLE DEVICE | Oct 23, 1987 | Substantially Equivalent |
| K864784 | SERAFLO(TM) BLOODLINES FOR HEMODIALYSIS | Jan 20, 1987 | Substantially Equivalent |
| K862304 | DRAKE WILLOCK CENTRAL DIALYSATE DELIVERY SYSTEM | Sep 9, 1986 | Substantially Equivalent |
| K853513 | DRAKE WILLOCK 480 UF CONTROL IDALYSATE DELIVERY SY | Nov 6, 1985 | Substantially Equivalent |
| K844185 | MODIFIED C-DAK | Jan 3, 1985 | Substantially Equivalent |