FLUIDSHIELD CONE CLASSIC II SURG MASK W/SPLASH VIS
K-Number: K911907 · 1991-07-08
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Device Summary
Frequently Asked Questions
What is the FLUIDSHIELD CONE CLASSIC II SURG MASK W/SPLASH VIS?
FLUIDSHIELD CONE CLASSIC II SURG MASK W/SPLASH VIS is a medical device that received FDA 510(k) clearance on 1991-07-08. The listed applicant is Tecnol New Jersey Wound Care, Inc.. The 510(k) number is K911907.
When did FLUIDSHIELD CONE CLASSIC II SURG MASK W/SPLASH VIS receive FDA 510(k) clearance?
FLUIDSHIELD CONE CLASSIC II SURG MASK W/SPLASH VIS received FDA 510(k) clearance on 1991-07-08, under 510(k) number K911907.
Who is the listed applicant for FLUIDSHIELD CONE CLASSIC II SURG MASK W/SPLASH VIS?
The FDA 510(k) record lists Tecnol New Jersey Wound Care, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLUIDSHIELD CONE CLASSIC II SURG MASK W/SPLASH VIS?
The FDA product code for FLUIDSHIELD CONE CLASSIC II SURG MASK W/SPLASH VIS is FXX.
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 Tecnol New Jersey Wound Care, 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: FXX)
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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