FDA 510(k)

HEPARIN CONTROL PLASMA

K-Number: K760918 · 1977-01-10

ApplicantHyland Therapeutic Div., Travenol Laboratories

Decision Date1977-01-10

Product CodeGFO

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

HEPARIN CONTROL PLASMA is the device name listed in this FDA 510(k) record. The listed applicant is Hyland Therapeutic Div., Travenol Laboratories. It received FDA 510(k) clearance on 1977-01-10 under 510(k) number K760918. The device is classified under product code GFO. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEPARIN CONTROL PLASMA?

HEPARIN CONTROL PLASMA is a medical device that received FDA 510(k) clearance on 1977-01-10. The listed applicant is Hyland Therapeutic Div., Travenol Laboratories. The 510(k) number is K760918.

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

HEPARIN CONTROL PLASMA received FDA 510(k) clearance on 1977-01-10, under 510(k) number K760918.

Who is the listed applicant for HEPARIN CONTROL PLASMA?

The FDA 510(k) record lists Hyland Therapeutic Div., Travenol Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEPARIN CONTROL PLASMA?

The FDA product code for HEPARIN CONTROL PLASMA is GFO.

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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.