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FDA 510(k)

ENURESIS ALARM

K-Number: K871787 · 1987-08-10

ApplicantDilorenzo Engineering Co.
Decision Date1987-08-10
Product CodeKPN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENURESIS ALARM is the device name listed in this FDA 510(k) record. The listed applicant is Dilorenzo Engineering Co.. It received FDA 510(k) clearance on 1987-08-10 under 510(k) number K871787. 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 ENURESIS ALARM?

ENURESIS ALARM is a medical device that received FDA 510(k) clearance on 1987-08-10. The listed applicant is Dilorenzo Engineering Co.. The 510(k) number is K871787.

When did ENURESIS ALARM receive FDA 510(k) clearance?

ENURESIS ALARM received FDA 510(k) clearance on 1987-08-10, under 510(k) number K871787.

Who is the listed applicant for ENURESIS ALARM?

The FDA 510(k) record lists Dilorenzo Engineering Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENURESIS ALARM?

The FDA product code for ENURESIS ALARM is KPN.

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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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