SENSICARE -C SYNTHETIC POLYISOPRENE POWDER-FREE SURGICAL GLOVES
K-Number: K023236 · 2002-11-12
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Device Summary
Frequently Asked Questions
What is the SENSICARE -C SYNTHETIC POLYISOPRENE POWDER-FREE SURGICAL GLOVES?
SENSICARE -C SYNTHETIC POLYISOPRENE POWDER-FREE SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 2002-11-12. The listed applicant is Maxxim Medical. The 510(k) number is K023236.
When did SENSICARE -C SYNTHETIC POLYISOPRENE POWDER-FREE SURGICAL GLOVES receive FDA 510(k) clearance?
SENSICARE -C SYNTHETIC POLYISOPRENE POWDER-FREE SURGICAL GLOVES received FDA 510(k) clearance on 2002-11-12, under 510(k) number K023236.
Who is the listed applicant for SENSICARE -C SYNTHETIC POLYISOPRENE POWDER-FREE SURGICAL GLOVES?
The FDA 510(k) record lists Maxxim Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SENSICARE -C SYNTHETIC POLYISOPRENE POWDER-FREE SURGICAL GLOVES?
The FDA product code for SENSICARE -C SYNTHETIC POLYISOPRENE POWDER-FREE SURGICAL GLOVES is KGO.
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 Maxxim Medical 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: KGO)
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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