MCLEAN-STOCK PERCUTANEOUS T-TUBE SET
K-Number: K921654 · 1992-07-02
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Device Summary
Frequently Asked Questions
What is the MCLEAN-STOCK PERCUTANEOUS T-TUBE SET?
MCLEAN-STOCK PERCUTANEOUS T-TUBE SET is a medical device that received FDA 510(k) clearance on 1992-07-02. The listed applicant is Cook, Inc.. The 510(k) number is K921654.
When did MCLEAN-STOCK PERCUTANEOUS T-TUBE SET receive FDA 510(k) clearance?
MCLEAN-STOCK PERCUTANEOUS T-TUBE SET received FDA 510(k) clearance on 1992-07-02, under 510(k) number K921654.
Who is the listed applicant for MCLEAN-STOCK PERCUTANEOUS T-TUBE SET?
The FDA 510(k) record lists Cook, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MCLEAN-STOCK PERCUTANEOUS T-TUBE SET?
The FDA product code for MCLEAN-STOCK PERCUTANEOUS T-TUBE SET is FGE.
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 Cook, 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: FGE)
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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