ENTROSET-SW
K-Number: K871003 · 1987-06-04
Advertisement
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement