INTRAVENOUS INJECTION SET
K-Number: K841717 · 1984-07-23
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Device Summary
Frequently Asked Questions
What is the INTRAVENOUS INJECTION SET?
INTRAVENOUS INJECTION SET is a medical device that received FDA 510(k) clearance on 1984-07-23. The listed applicant is Philadelphia Biologics Center. The 510(k) number is K841717.
When did INTRAVENOUS INJECTION SET receive FDA 510(k) clearance?
INTRAVENOUS INJECTION SET received FDA 510(k) clearance on 1984-07-23, under 510(k) number K841717.
Who is the listed applicant for INTRAVENOUS INJECTION SET?
The FDA 510(k) record lists Philadelphia Biologics Center as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTRAVENOUS INJECTION SET?
The FDA product code for INTRAVENOUS INJECTION 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 Philadelphia Biologics Center 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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