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FDA 510(k)

ENTROSET-SW

K-Number: K871003 · 1987-06-04

Decision Date1987-06-04
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENTROSET-SW is the device name listed in this FDA 510(k) record. The listed applicant is White River (Tm). It received FDA 510(k) clearance on 1987-06-04 under 510(k) number K871003. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENTROSET-SW?

ENTROSET-SW is a medical device that received FDA 510(k) clearance on 1987-06-04. The listed applicant is White River (Tm). The 510(k) number is K871003.

When did ENTROSET-SW receive FDA 510(k) clearance?

ENTROSET-SW received FDA 510(k) clearance on 1987-06-04, under 510(k) number K871003.

Who is the listed applicant for ENTROSET-SW?

The FDA 510(k) record lists White River (Tm) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENTROSET-SW?

The FDA product code for ENTROSET-SW is KNT.

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 White River (Tm) 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: KNT)

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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