CONTINU-FLO SOLUTION SET
K-Number: K971701 · 1997-06-06
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Device Summary
Frequently Asked Questions
What is the CONTINU-FLO SOLUTION SET?
CONTINU-FLO SOLUTION SET is a medical device that received FDA 510(k) clearance on 1997-06-06. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K971701.
When did CONTINU-FLO SOLUTION SET receive FDA 510(k) clearance?
CONTINU-FLO SOLUTION SET received FDA 510(k) clearance on 1997-06-06, under 510(k) number K971701.
Who is the listed applicant for CONTINU-FLO 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 SOLUTION SET?
The FDA product code for CONTINU-FLO 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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