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)

SAFE T RETRACTABLE BLOOD COLLECTION DEVICE

K-Number: K041941 · 2004-09-13

Decision Date2004-09-13
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SAFE T RETRACTABLE BLOOD COLLECTION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Safe T Medical Devices, Ltd.. It received FDA 510(k) clearance on 2004-09-13 under 510(k) number K041941. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAFE T RETRACTABLE BLOOD COLLECTION DEVICE?

SAFE T RETRACTABLE BLOOD COLLECTION DEVICE is a medical device that received FDA 510(k) clearance on 2004-09-13. The listed applicant is Safe T Medical Devices, Ltd.. The 510(k) number is K041941.

When did SAFE T RETRACTABLE BLOOD COLLECTION DEVICE receive FDA 510(k) clearance?

SAFE T RETRACTABLE BLOOD COLLECTION DEVICE received FDA 510(k) clearance on 2004-09-13, under 510(k) number K041941.

Who is the listed applicant for SAFE T RETRACTABLE BLOOD COLLECTION DEVICE?

The FDA 510(k) record lists Safe T Medical Devices, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAFE T RETRACTABLE BLOOD COLLECTION DEVICE?

The FDA product code for SAFE T RETRACTABLE BLOOD COLLECTION DEVICE is FMI.

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.

Related Devices (Code: FMI)

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.

↑