PROXCELAN CS-131 PRELOADED BRAIDED STRANDS, MODEL: PL-5
K-Number: K092136 · 2009-08-07
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Device Summary
Frequently Asked Questions
What is the PROXCELAN CS-131 PRELOADED BRAIDED STRANDS, MODEL: PL-5?
PROXCELAN CS-131 PRELOADED BRAIDED STRANDS, MODEL: PL-5 is a medical device that received FDA 510(k) clearance on 2009-08-07. The listed applicant is Isoray Medical, Inc.. The 510(k) number is K092136.
When did PROXCELAN CS-131 PRELOADED BRAIDED STRANDS, MODEL: PL-5 receive FDA 510(k) clearance?
PROXCELAN CS-131 PRELOADED BRAIDED STRANDS, MODEL: PL-5 received FDA 510(k) clearance on 2009-08-07, under 510(k) number K092136.
Who is the listed applicant for PROXCELAN CS-131 PRELOADED BRAIDED STRANDS, MODEL: PL-5?
The FDA 510(k) record lists Isoray Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROXCELAN CS-131 PRELOADED BRAIDED STRANDS, MODEL: PL-5?
The FDA product code for PROXCELAN CS-131 PRELOADED BRAIDED STRANDS, MODEL: PL-5 is KXK.
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 Isoray Medical, 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: KXK)
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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