SUCTION CATHETER TRAY PRODUCT NO. 900277
K-Number: K964011 · 1996-11-25
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Device Summary
Frequently Asked Questions
What is the SUCTION CATHETER TRAY PRODUCT NO. 900277?
SUCTION CATHETER TRAY PRODUCT NO. 900277 is a medical device that received FDA 510(k) clearance on 1996-11-25. The listed applicant is Customed, Inc.. The 510(k) number is K964011.
When did SUCTION CATHETER TRAY PRODUCT NO. 900277 receive FDA 510(k) clearance?
SUCTION CATHETER TRAY PRODUCT NO. 900277 received FDA 510(k) clearance on 1996-11-25, under 510(k) number K964011.
Who is the listed applicant for SUCTION CATHETER TRAY PRODUCT NO. 900277?
The FDA 510(k) record lists Customed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUCTION CATHETER TRAY PRODUCT NO. 900277?
The FDA product code for SUCTION CATHETER TRAY PRODUCT NO. 900277 is LRO.
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 Customed, 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: LRO)
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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