SELECT-A-FLOW
K-Number: K811857 · 1981-07-10
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Device Summary
Frequently Asked Questions
What is the SELECT-A-FLOW?
SELECT-A-FLOW is a medical device that received FDA 510(k) clearance on 1981-07-10. The listed applicant is Wenmar Intl. Corp.. The 510(k) number is K811857.
When did SELECT-A-FLOW receive FDA 510(k) clearance?
SELECT-A-FLOW received FDA 510(k) clearance on 1981-07-10, under 510(k) number K811857.
Who is the listed applicant for SELECT-A-FLOW?
The FDA 510(k) record lists Wenmar Intl. Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SELECT-A-FLOW?
The FDA product code for SELECT-A-FLOW is KNK.
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 Wenmar Intl. 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: KNK)
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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