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FDA 510(k)

CHECK VALVE SOLUTION SET

K-Number: K941453 · 1994-08-16

Decision Date1994-08-16
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CHECK VALVE SOLUTION SET is the device name listed in this FDA 510(k) record. The listed applicant is Douglas Medical Products Corp.. It received FDA 510(k) clearance on 1994-08-16 under 510(k) number K941453. 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 CHECK VALVE SOLUTION SET?

CHECK VALVE SOLUTION SET is a medical device that received FDA 510(k) clearance on 1994-08-16. The listed applicant is Douglas Medical Products Corp.. The 510(k) number is K941453.

When did CHECK VALVE SOLUTION SET receive FDA 510(k) clearance?

CHECK VALVE SOLUTION SET received FDA 510(k) clearance on 1994-08-16, under 510(k) number K941453.

Who is the listed applicant for CHECK VALVE SOLUTION SET?

The FDA 510(k) record lists Douglas Medical Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHECK VALVE SOLUTION SET?

The FDA product code for CHECK VALVE 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 Douglas Medical Products 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 19 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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