TUBE DECLOGGER
K-Number: K905164 · 1991-02-13
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Device Summary
Frequently Asked Questions
What is the TUBE DECLOGGER?
TUBE DECLOGGER is a medical device that received FDA 510(k) clearance on 1991-02-13. The listed applicant is Nova Design Technologies, Ltd.. The 510(k) number is K905164.
When did TUBE DECLOGGER receive FDA 510(k) clearance?
TUBE DECLOGGER received FDA 510(k) clearance on 1991-02-13, under 510(k) number K905164.
Who is the listed applicant for TUBE DECLOGGER?
The FDA 510(k) record lists Nova Design Technologies, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TUBE DECLOGGER?
The FDA product code for TUBE DECLOGGER 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.
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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