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FDA 510(k)

CRP-ADVANCE MULTI CALIBRATOR SET, MODEL SE-250

K-Number: K060140 · 2006-04-24

ApplicantDiagnostic Chemicals , Ltd.
Decision Date2006-04-24
Product CodeJIT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CRP-ADVANCE MULTI CALIBRATOR SET, MODEL SE-250 is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Chemicals , Ltd.. It received FDA 510(k) clearance on 2006-04-24 under 510(k) number K060140. The device is classified under product code JIT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRP-ADVANCE MULTI CALIBRATOR SET, MODEL SE-250?

CRP-ADVANCE MULTI CALIBRATOR SET, MODEL SE-250 is a medical device that received FDA 510(k) clearance on 2006-04-24. The listed applicant is Diagnostic Chemicals , Ltd.. The 510(k) number is K060140.

When did CRP-ADVANCE MULTI CALIBRATOR SET, MODEL SE-250 receive FDA 510(k) clearance?

CRP-ADVANCE MULTI CALIBRATOR SET, MODEL SE-250 received FDA 510(k) clearance on 2006-04-24, under 510(k) number K060140.

Who is the listed applicant for CRP-ADVANCE MULTI CALIBRATOR SET, MODEL SE-250?

The FDA 510(k) record lists Diagnostic Chemicals , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CRP-ADVANCE MULTI CALIBRATOR SET, MODEL SE-250?

The FDA product code for CRP-ADVANCE MULTI CALIBRATOR SET, MODEL SE-250 is JIT.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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