Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SPLASH MASK

K-Number: K941932 · 1994-07-19

ApplicantIncon Diversified Industries, Inc.
Decision Date1994-07-19
Product CodeLYU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SPLASH MASK is the device name listed in this FDA 510(k) record. The listed applicant is Incon Diversified Industries, Inc.. It received FDA 510(k) clearance on 1994-07-19 under 510(k) number K941932. 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 SPLASH MASK?

SPLASH MASK is a medical device that received FDA 510(k) clearance on 1994-07-19. The listed applicant is Incon Diversified Industries, Inc.. The 510(k) number is K941932.

When did SPLASH MASK receive FDA 510(k) clearance?

SPLASH MASK received FDA 510(k) clearance on 1994-07-19, under 510(k) number K941932.

Who is the listed applicant for SPLASH MASK?

The FDA 510(k) record lists Incon Diversified Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPLASH MASK?

The FDA product code for SPLASH MASK is LYU.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

↑