LONG MEDIUM PALMAZ-SCHATZ BALLOON EXPANDABLE STENT
K-Number: K964688 · 1997-06-20
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Device Summary
Frequently Asked Questions
What is the LONG MEDIUM PALMAZ-SCHATZ BALLOON EXPANDABLE STENT?
LONG MEDIUM PALMAZ-SCHATZ BALLOON EXPANDABLE STENT is a medical device that received FDA 510(k) clearance on 1997-06-20. The listed applicant is Cordis Corp.. The 510(k) number is K964688.
When did LONG MEDIUM PALMAZ-SCHATZ BALLOON EXPANDABLE STENT receive FDA 510(k) clearance?
LONG MEDIUM PALMAZ-SCHATZ BALLOON EXPANDABLE STENT received FDA 510(k) clearance on 1997-06-20, under 510(k) number K964688.
Who is the listed applicant for LONG MEDIUM PALMAZ-SCHATZ BALLOON EXPANDABLE STENT?
The FDA 510(k) record lists Cordis Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LONG MEDIUM PALMAZ-SCHATZ BALLOON EXPANDABLE STENT?
The FDA product code for LONG MEDIUM PALMAZ-SCHATZ BALLOON EXPANDABLE STENT 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 Cordis 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: 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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