CORRUGATED FLEX TUBING
K-Number: K810362 · 1981-03-17
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Device Summary
Frequently Asked Questions
What is the CORRUGATED FLEX TUBING?
CORRUGATED FLEX TUBING is a medical device that received FDA 510(k) clearance on 1981-03-17. The listed applicant is Todd Industries, Inc.. The 510(k) number is K810362.
When did CORRUGATED FLEX TUBING receive FDA 510(k) clearance?
CORRUGATED FLEX TUBING received FDA 510(k) clearance on 1981-03-17, under 510(k) number K810362.
Who is the listed applicant for CORRUGATED FLEX TUBING?
The FDA 510(k) record lists Todd Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CORRUGATED FLEX TUBING?
The FDA product code for CORRUGATED FLEX 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 Todd 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: 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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