Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

HEPARIN CONTROL KIT

K-Number: K943520 · 1995-09-26

Decision Date1995-09-26
Product CodeKFF
Advisory CommitteeHE
DecisionUnknown

Device Summary

HEPARIN CONTROL KIT is the device name listed in this FDA 510(k) record. The listed applicant is American Bioproducts Co.. It received FDA 510(k) clearance on 1995-09-26 under 510(k) number K943520. The device is classified under product code KFF. It was reviewed by the HE advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the HEPARIN CONTROL KIT?

HEPARIN CONTROL KIT is a medical device that received FDA 510(k) clearance on 1995-09-26. The listed applicant is American Bioproducts Co.. The 510(k) number is K943520.

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

HEPARIN CONTROL KIT received FDA 510(k) clearance on 1995-09-26, under 510(k) number K943520.

Who is the listed applicant for HEPARIN CONTROL KIT?

The FDA 510(k) record lists American Bioproducts Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEPARIN CONTROL KIT?

The FDA product code for HEPARIN CONTROL KIT is KFF.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing American Bioproducts Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 79 devices →

Related Devices (Code: KFF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

↑