CONTINU-FLO(R) SOLUTION SET
K-Number: K921703 · 1992-06-04
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Device Summary
Frequently Asked Questions
What is the CONTINU-FLO(R) SOLUTION SET?
CONTINU-FLO(R) SOLUTION SET is a medical device that received FDA 510(k) clearance on 1992-06-04. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K921703.
When did CONTINU-FLO(R) SOLUTION SET receive FDA 510(k) clearance?
CONTINU-FLO(R) SOLUTION SET received FDA 510(k) clearance on 1992-06-04, under 510(k) number K921703.
Who is the listed applicant for CONTINU-FLO(R) SOLUTION SET?
The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONTINU-FLO(R) SOLUTION SET?
The FDA product code for CONTINU-FLO(R) SOLUTION 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 Baxter Healthcare Corp 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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