DENLEY WELLDILL 3
K-Number: K894272 · 1989-08-21
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Device Summary
Frequently Asked Questions
What is the DENLEY WELLDILL 3?
DENLEY WELLDILL 3 is a medical device that received FDA 510(k) clearance on 1989-08-21. The listed applicant is Denley Instruments, Inc.. The 510(k) number is K894272.
When did DENLEY WELLDILL 3 receive FDA 510(k) clearance?
DENLEY WELLDILL 3 received FDA 510(k) clearance on 1989-08-21, under 510(k) number K894272.
Who is the listed applicant for DENLEY WELLDILL 3?
The FDA 510(k) record lists Denley Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DENLEY WELLDILL 3?
The FDA product code for DENLEY WELLDILL 3 is JQW.
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 Denley Instruments, 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: JQW)
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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