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FDA 510(k)

SELECT-A-FLOW

K-Number: K811857 · 1981-07-10

Decision Date1981-07-10
Product CodeKNK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SELECT-A-FLOW is the device name listed in this FDA 510(k) record. The listed applicant is Wenmar Intl. Corp.. It received FDA 510(k) clearance on 1981-07-10 under 510(k) number K811857. The device is classified under product code KNK. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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