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FDA 510(k)

FLUIDSHIELD CONE CLASSIC II SURG MASK W/SPLASH VIS

K-Number: K911907 · 1991-07-08

Decision Date1991-07-08
Product CodeFXX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FLUIDSHIELD CONE CLASSIC II SURG MASK W/SPLASH VIS is the device name listed in this FDA 510(k) record. The listed applicant is Tecnol New Jersey Wound Care, Inc.. It received FDA 510(k) clearance on 1991-07-08 under 510(k) number K911907. The device is classified under product code FXX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 35 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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