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FDA 510(k)

WET-NO-MORE MONITOR

K-Number: K901906 · 1990-07-11

ApplicantTravis Industries, Inc.
Decision Date1990-07-11
Product CodeKPN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

WET-NO-MORE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Travis Industries, Inc.. It received FDA 510(k) clearance on 1990-07-11 under 510(k) number K901906. The device is classified under product code KPN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WET-NO-MORE MONITOR?

WET-NO-MORE MONITOR is a medical device that received FDA 510(k) clearance on 1990-07-11. The listed applicant is Travis Industries, Inc.. The 510(k) number is K901906.

When did WET-NO-MORE MONITOR receive FDA 510(k) clearance?

WET-NO-MORE MONITOR received FDA 510(k) clearance on 1990-07-11, under 510(k) number K901906.

Who is the listed applicant for WET-NO-MORE MONITOR?

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

What is the FDA product code for WET-NO-MORE MONITOR?

The FDA product code for WET-NO-MORE MONITOR is KPN.

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

Other records listing Travis Industries, 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.

K903856WET-NO-MORE MONITORK901907PROFESSIONAL MONITOR

Related Devices (Code: KPN)

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.

K130951SIMSimavita Pty LimitedK971442HUGHES BLADDER AND BOWEL TRAINING SYSTEM(AD-T-18, MED-18,MED-1,MED-T-1,MEDD-18,MED-38,MED-T-10,MED-T-25,MED-T-5Humed, Inc.K971855POTTY PAL AND FOREVER-DRYDigital Applications, Inc.K962770UROSURGE ACUTRAINERPrinceton Regulatory Assoc.K962416DRYTIME FOR BLADDER CONTROL SILENTBio-Systems ResearchK955338DRYTIME FOR POTTY TRAININGHealth Sense Intl., 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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