SCHNEIDER WALLSTENT(R)
K-Number: K911292 · 1991-05-01
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Device Summary
Frequently Asked Questions
What is the SCHNEIDER WALLSTENT(R)?
SCHNEIDER WALLSTENT(R) is a medical device that received FDA 510(k) clearance on 1991-05-01. The listed applicant is Pfizer Hospital Products Group, Inc.. The 510(k) number is K911292.
When did SCHNEIDER WALLSTENT(R) receive FDA 510(k) clearance?
SCHNEIDER WALLSTENT(R) received FDA 510(k) clearance on 1991-05-01, under 510(k) number K911292.
Who is the listed applicant for SCHNEIDER WALLSTENT(R)?
The FDA 510(k) record lists Pfizer Hospital Products Group, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SCHNEIDER WALLSTENT(R)?
The FDA product code for SCHNEIDER WALLSTENT(R) 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 Pfizer Hospital Products Group, 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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