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FDA 510(k)

CONTINU-FLO(R) SOLUTION SET

K-Number: K921703 · 1992-06-04

Decision Date1992-06-04
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CONTINU-FLO(R) SOLUTION SET is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1992-06-04 under 510(k) number K921703. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 504 devices →

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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