Acid, Uric, Uricase (Colorimetric)
FDA product code KNK · 118 cleared devices
Class 1
Clinical Chemistry
- Regulation
- 21 CFR 862.1775
- Review panel
- CH
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1977-03-01 – 2011-05-06
KNK
1981-07-10
KNK
1981-07-01
URIC ACID TEST
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KNK
1981-06-09
WAKO URIC ACID B TEST
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KNK
1981-02-02
URIC ACID REAGENT SYSTEM
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KNK
1980-12-10
AMES SERA-PAK URIC ACID REAGENT KIT
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KNK
1980-12-10
LANCER URIC ACID AUTO/STAT KIT
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KNK
1980-10-10
URIC ACID DIAGNOSTIC REAGENT
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KNK
1980-08-20
KODAK EKTACHEM CLINICAL CHEMISTRY SLIDES
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KNK
1980-04-24
SERALYZER URIC ACID REAGENT STRIPS -
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KNK
1980-01-29
URIC ACID KIT
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KNK
1979-09-27
URIC ACID REAGENT
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KNK
1979-07-30
URIDROP SPECIAL
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KNK
1979-04-23
FLOZYME* URIC ACID REAGENT
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KNK
1979-03-12
URIC ACID, BOUND ENZYME
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KNK
1978-07-27
HMA URIC ACID TEST
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KNK
1978-06-13
URIC ACID RAPID STAT KIT
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KNK
1977-07-21
UNIPAK URIC ACID
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KNK
1977-03-01
URIC ACID TEST, BMC AUTOFLO
View details →No matching devices.
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