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)

SHAMROCK SAFETY BLOOD COLLECTION SET

K-Number: K895705 · 1989-10-10

Decision Date1989-10-10
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHAMROCK SAFETY BLOOD COLLECTION SET is the device name listed in this FDA 510(k) record. The listed applicant is Ryan Medical, Inc.. It received FDA 510(k) clearance on 1989-10-10 under 510(k) number K895705. 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 SHAMROCK SAFETY BLOOD COLLECTION SET?

SHAMROCK SAFETY BLOOD COLLECTION SET is a medical device that received FDA 510(k) clearance on 1989-10-10. The listed applicant is Ryan Medical, Inc.. The 510(k) number is K895705.

When did SHAMROCK SAFETY BLOOD COLLECTION SET receive FDA 510(k) clearance?

SHAMROCK SAFETY BLOOD COLLECTION SET received FDA 510(k) clearance on 1989-10-10, under 510(k) number K895705.

Who is the listed applicant for SHAMROCK SAFETY BLOOD COLLECTION SET?

The FDA 510(k) record lists Ryan Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHAMROCK SAFETY BLOOD COLLECTION SET?

The FDA product code for SHAMROCK SAFETY BLOOD COLLECTION SET 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.

Other records listing Ryan Medical, Inc. 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.

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.

↑