THREE FLUID I.V. SETS
K-Number: K871841 · 1987-06-24
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Device Summary
Frequently Asked Questions
What is the THREE FLUID I.V. SETS?
THREE FLUID I.V. SETS is a medical device that received FDA 510(k) clearance on 1987-06-24. The listed applicant is Panamedix, Inc.. The 510(k) number is K871841.
When did THREE FLUID I.V. SETS receive FDA 510(k) clearance?
THREE FLUID I.V. SETS received FDA 510(k) clearance on 1987-06-24, under 510(k) number K871841.
Who is the listed applicant for THREE FLUID I.V. SETS?
The FDA 510(k) record lists Panamedix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THREE FLUID I.V. SETS?
The FDA product code for THREE FLUID I.V. SETS 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 Panamedix, 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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