Abx Pentra Enzymatic Creatinine CP, Abx Pentra Multical, Abx Pentra N Control, Abx Pentra P Control, and Abx Pentra Urin

FDA 510(k) K110137 · Horiba Abx SAS

Substantially Equivalent

510(k) numberK110137

Submission

Device name
Abx Pentra Enzymatic Creatinine CP, Abx Pentra Multical, Abx Pentra N Control, Abx Pentra P Control, and Abx Pentra Urin
Applicant
Horiba Abx SAS
Montpellier, FR
Received
January 18, 2011
Decision date
August 10, 2011
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JFY – Enzymatic Method, Creatinine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1225
Specialty
Clinical Chemistry

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More from ACON Laboratories, Inc.

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K192028Yumizen C1200 CRPDCK · Traditional 06/25/2020SE
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K191245Yumizen C1200 ALP, Yumizen C1200 AlbuminCJE · Traditional 08/30/2019SE
K191396Yumizen C1200 Calcium AS, Yumizen C1200 Creatinine JaffeCJY · Traditional 07/26/2019SE
K170353ABX MICROS ES 60 OT and ABX MICROS ES 60 CTGKZ · Traditional 11/01/2017SE
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Questions and answers

When was Abx Pentra Enzymatic Creatinine CP, Abx Pentra Multical, Abx Pentra N Control, Abx Pentra P Control, and Abx Pentra Urin cleared by the FDA?

Abx Pentra Enzymatic Creatinine CP, Abx Pentra Multical, Abx Pentra N Control, Abx Pentra P Control, and Abx Pentra Urin (K110137) received a 510(k) decision of Substantially Equivalent on August 10, 2011, 204 days after the submission was received.

What is the product code of K110137?

The FDA product code is JFY – Enzymatic Method, Creatinine, a Class II (moderate risk) device regulated under 21 CFR 862.1225.