CONNECTING TUBING
K-Number: K831082 · 1983-05-09
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Device Summary
Frequently Asked Questions
What is the CONNECTING TUBING?
CONNECTING TUBING is a medical device that received FDA 510(k) clearance on 1983-05-09. The listed applicant is The Kendall Company Div. of Tyco Healthcare Group. The 510(k) number is K831082.
When did CONNECTING TUBING receive FDA 510(k) clearance?
CONNECTING TUBING received FDA 510(k) clearance on 1983-05-09, under 510(k) number K831082.
Who is the listed applicant for CONNECTING TUBING?
The FDA 510(k) record lists The Kendall Company Div. of Tyco Healthcare Group as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONNECTING TUBING?
The FDA product code for CONNECTING TUBING is BYX.
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 The Kendall Company Div. of Tyco Healthcare Group 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: BYX)
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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