FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ULTRAZYME PLUS CKI, #64978,65027&65028

K Number: K821473 · Decision Jun 3, 1982
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
122
Applicant Total
62
Review Days
16

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Basic Information

Device Name
ULTRAZYME PLUS CKI, #64978,65027&65028
K Number
K821473
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Emd Chemicals, Inc.
Date Received
May 18, 1982
Decision Date
June 3, 1982
Product Code
CGS
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
CGS Nad Reduction/Nadh Oxidation, Cpk Or Isoenzymes

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K Number Device Name
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K981926 ETHYL ALCOHOL CLINICAL STANDARD SOLUTIONS
K973054 ETHYL ALCOHOL CLINICAL STANDARD SOLUTIONS
K951494 AMYLASE TEST ITEM 97381/94 (R1, 97382/94 (R2-SR)
K951750 GLUCOSE TEST ITEM NUMBER 97375/94
K950234 TOTAL PROTEIN TEST (TPRO) ITEM NUMBER: XXXXX/R1. R2
K950128 TOTAL PROTEIN TEST (TPRO) ITEM XXXXX/R1. R2
K945322 PHOSPHORUS TEST (PHOS) ITEM NUMBER 65416
K945368 PHOSPHORUS TEST (PHOS)
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