ENTEROCYSIS TUBE W/GUIDE WIRE & CONNECT
K-Number: K840752 · 1984-05-02
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Device Summary
Frequently Asked Questions
What is the ENTEROCYSIS TUBE W/GUIDE WIRE & CONNECT?
ENTEROCYSIS TUBE W/GUIDE WIRE & CONNECT is a medical device that received FDA 510(k) clearance on 1984-05-02. The listed applicant is E-Z-Em, Inc.. The 510(k) number is K840752.
When did ENTEROCYSIS TUBE W/GUIDE WIRE & CONNECT receive FDA 510(k) clearance?
ENTEROCYSIS TUBE W/GUIDE WIRE & CONNECT received FDA 510(k) clearance on 1984-05-02, under 510(k) number K840752.
Who is the listed applicant for ENTEROCYSIS TUBE W/GUIDE WIRE & CONNECT?
The FDA 510(k) record lists E-Z-Em, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENTEROCYSIS TUBE W/GUIDE WIRE & CONNECT?
The FDA product code for ENTEROCYSIS TUBE W/GUIDE WIRE & CONNECT 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 E-Z-Em, Inc. 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.
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