FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
KEMBLE LIQUID HANDLING SYSTEM DISPENSER
K Number: K896684
·
Decision Apr 16, 1990
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
139
Applicant Total
15
Review Days
139
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Basic Information
- Device Name
- KEMBLE LIQUID HANDLING SYSTEM DISPENSER
- K Number
- K896684
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.2750
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Schiff & Co.
- Date Received
- November 28, 1989
- Decision Date
- April 16, 1990
- Product Code
- JQW
- Advisory Committee
- Clinical Chemistry
- Review Advisory Committee
- CH
- 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 |
|---|---|---|---|
| JQW | Station, Pipetting And Diluting, For Clinical Use | FDA class 1 | Clinical Chemistry |
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|---|---|---|---|
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| K981629 | NUTRISAFE ENTERAL FEEDING TUBE | Feb 4, 1999 | Substantially Equivalent |
| K981630 | VYGON DOUBLE LUMEN UMBILICAL CATHETER | Oct 1, 1998 | Substantially Equivalent |
| K974141 | PLUS REUSABLE RESUSCITATOR | May 21, 1998 | Substantially Equivalent |
| K954448 | VIOTEC V-2200 ULTRAVIOLET GERMICIDAL AIR PURIFICATION SYSTEM | Oct 28, 1996 | Substantially Equivalent |
| K955085 | HM-CAP EIA TEST (MODIFICATION) | Feb 9, 1996 | Substantially Equivalent |
| K944159 | HM-CAP EIA KIT | Jul 18, 1995 | Substantially Equivalent |
| K943521 | VIOTEC 1400 SERIES ULTRAVIOLET GERMICIDAL FIXTURE | Feb 14, 1995 | Substantially Equivalent |
| K894617 | OLYMPUS PK-TP SYSTEM REACTIVE CONTROL | Oct 31, 1989 | Substantially Equivalent |