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FDA 510(k)

SENTRY SIGNAL ENURESIS ALARM SYSTEM

K-Number: K844636 · 1985-04-03

ApplicantConklin Technology, Inc.
Decision Date1985-04-03
Product CodeKPN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SENTRY SIGNAL ENURESIS ALARM SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Conklin Technology, Inc.. It received FDA 510(k) clearance on 1985-04-03 under 510(k) number K844636. 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 SENTRY SIGNAL ENURESIS ALARM SYSTEM?

SENTRY SIGNAL ENURESIS ALARM SYSTEM is a medical device that received FDA 510(k) clearance on 1985-04-03. The listed applicant is Conklin Technology, Inc.. The 510(k) number is K844636.

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

SENTRY SIGNAL ENURESIS ALARM SYSTEM received FDA 510(k) clearance on 1985-04-03, under 510(k) number K844636.

Who is the listed applicant for SENTRY SIGNAL ENURESIS ALARM SYSTEM?

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

What is the FDA product code for SENTRY SIGNAL ENURESIS ALARM SYSTEM?

The FDA product code for SENTRY SIGNAL ENURESIS ALARM SYSTEM 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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