DYNACOR CONNECTING TUBING
K-Number: K832398 · 1983-08-24
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Device Summary
Frequently Asked Questions
What is the DYNACOR CONNECTING TUBING?
DYNACOR CONNECTING TUBING is a medical device that received FDA 510(k) clearance on 1983-08-24. The listed applicant is Medline Industries, Inc.. The 510(k) number is K832398.
When did DYNACOR CONNECTING TUBING receive FDA 510(k) clearance?
DYNACOR CONNECTING TUBING received FDA 510(k) clearance on 1983-08-24, under 510(k) number K832398.
Who is the listed applicant for DYNACOR CONNECTING TUBING?
The FDA 510(k) record lists Medline Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DYNACOR CONNECTING TUBING?
The FDA product code for DYNACOR CONNECTING TUBING is BYY.
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 Medline Industries, 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: BYY)
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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