PERRY(R) ENCORE CHEMOTHERAPY GLOVE
K-Number: K911633 · 1991-05-09
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Device Summary
Frequently Asked Questions
What is the PERRY(R) ENCORE CHEMOTHERAPY GLOVE?
PERRY(R) ENCORE CHEMOTHERAPY GLOVE is a medical device that received FDA 510(k) clearance on 1991-05-09. The listed applicant is Smith & Nephew Perry. The 510(k) number is K911633.
When did PERRY(R) ENCORE CHEMOTHERAPY GLOVE receive FDA 510(k) clearance?
PERRY(R) ENCORE CHEMOTHERAPY GLOVE received FDA 510(k) clearance on 1991-05-09, under 510(k) number K911633.
Who is the listed applicant for PERRY(R) ENCORE CHEMOTHERAPY GLOVE?
The FDA 510(k) record lists Smith & Nephew Perry as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PERRY(R) ENCORE CHEMOTHERAPY GLOVE?
The FDA product code for PERRY(R) ENCORE CHEMOTHERAPY GLOVE is LYY.
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 Smith & Nephew Perry 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: LYY)
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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