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FDA 510(k)

CONTROL PLASMA LMW HEPARIN

K-Number: K030965 · 2003-06-06

ApplicantInstrumentation Laboratory CO
Decision Date2003-06-06
Product CodeGGN
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

CONTROL PLASMA LMW HEPARIN is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory CO. It received FDA 510(k) clearance on 2003-06-06 under 510(k) number K030965. The device is classified under product code GGN. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTROL PLASMA LMW HEPARIN?

CONTROL PLASMA LMW HEPARIN is a medical device that received FDA 510(k) clearance on 2003-06-06. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K030965.

When did CONTROL PLASMA LMW HEPARIN receive FDA 510(k) clearance?

CONTROL PLASMA LMW HEPARIN received FDA 510(k) clearance on 2003-06-06, under 510(k) number K030965.

Who is the listed applicant for CONTROL PLASMA LMW HEPARIN?

The FDA 510(k) record lists Instrumentation Laboratory CO as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONTROL PLASMA LMW HEPARIN?

The FDA product code for CONTROL PLASMA LMW HEPARIN is GGN.

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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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