SHAMROCK SAFETY WINGED INFUSION SET
K-Number: K895481 · 1989-10-10
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Device Summary
Frequently Asked Questions
What is the SHAMROCK SAFETY WINGED INFUSION SET?
SHAMROCK SAFETY WINGED INFUSION 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 K895481.
When did SHAMROCK SAFETY WINGED INFUSION SET receive FDA 510(k) clearance?
SHAMROCK SAFETY WINGED INFUSION SET received FDA 510(k) clearance on 1989-10-10, under 510(k) number K895481.
Who is the listed applicant for SHAMROCK SAFETY WINGED INFUSION 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 WINGED INFUSION SET?
The FDA product code for SHAMROCK SAFETY WINGED INFUSION SET is FPA.
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: FPA)
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.
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