CENTURION KLEEN-NEEDLE SYSTEM I.V. EXTENSION SETS
K-Number: K910906 · 1991-04-01
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Device Summary
Frequently Asked Questions
What is the CENTURION KLEEN-NEEDLE SYSTEM I.V. EXTENSION SETS?
CENTURION KLEEN-NEEDLE SYSTEM I.V. EXTENSION SETS is a medical device that received FDA 510(k) clearance on 1991-04-01. The listed applicant is Tri-State Hospital Supply Corp.. The 510(k) number is K910906.
When did CENTURION KLEEN-NEEDLE SYSTEM I.V. EXTENSION SETS receive FDA 510(k) clearance?
CENTURION KLEEN-NEEDLE SYSTEM I.V. EXTENSION SETS received FDA 510(k) clearance on 1991-04-01, under 510(k) number K910906.
Who is the listed applicant for CENTURION KLEEN-NEEDLE SYSTEM I.V. EXTENSION SETS?
The FDA 510(k) record lists Tri-State Hospital Supply Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CENTURION KLEEN-NEEDLE SYSTEM I.V. EXTENSION SETS?
The FDA product code for CENTURION KLEEN-NEEDLE SYSTEM I.V. EXTENSION SETS is FPK.
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 Tri-State Hospital Supply Corp. 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: FPK)
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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