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FDA 510(k)

AGAFAR FACE SHIELD

K-Number: K935779 · 1994-02-01

ApplicantInfection Control Products, Inc.
Decision Date1994-02-01
Product CodeLYU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AGAFAR FACE SHIELD is the device name listed in this FDA 510(k) record. The listed applicant is Infection Control Products, Inc.. It received FDA 510(k) clearance on 1994-02-01 under 510(k) number K935779. The device is classified under product code LYU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AGAFAR FACE SHIELD?

AGAFAR FACE SHIELD is a medical device that received FDA 510(k) clearance on 1994-02-01. The listed applicant is Infection Control Products, Inc.. The 510(k) number is K935779.

When did AGAFAR FACE SHIELD receive FDA 510(k) clearance?

AGAFAR FACE SHIELD received FDA 510(k) clearance on 1994-02-01, under 510(k) number K935779.

Who is the listed applicant for AGAFAR FACE SHIELD?

The FDA 510(k) record lists Infection Control Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AGAFAR FACE SHIELD?

The FDA product code for AGAFAR FACE SHIELD is LYU.

Related Clinical Trials

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Other records listing Infection Control Products, 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.

K900643FLUID SOAKERSHIELDK900644I.V. FREEDOM CLIPK9001754/1 ARMBOARD

Related Devices (Code: LYU)

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.

K011755STRYKER T4 HYTREL (R) TOGASStryker Corp.K965237NURSES BOUFFANT CAPCopioumed Intl., Inc.K970988FAR-EAST BOUFFANT CAPSFar East Science & Technology Development Co., Ltd.K964364DISPOSABLE APRONInstrument Makar, Inc.K961791DEPUY DISPOSABLE FILTER/HOODDepuy, Inc.K961454AMMI MAGNI-GUARDAmerican Medical Mfg., Inc.

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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