FDA 510(k)

DRY TIME

K-Number: K911279 · 1991-09-04

Decision Date1991-09-04

Product CodeKPN

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

DRY TIME is the device name listed in this FDA 510(k) record. The listed applicant is Health Sense Intl., Inc.. It received FDA 510(k) clearance on 1991-09-04 under 510(k) number K911279. 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 DRY TIME?

DRY TIME is a medical device that received FDA 510(k) clearance on 1991-09-04. The listed applicant is Health Sense Intl., Inc.. The 510(k) number is K911279.

When did DRY TIME receive FDA 510(k) clearance?

DRY TIME received FDA 510(k) clearance on 1991-09-04, under 510(k) number K911279.

Who is the listed applicant for DRY TIME?

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

What is the FDA product code for DRY TIME?

The FDA product code for DRY TIME is KPN.

Other records listing Health Sense Intl., 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.

K955338DRYTIME FOR POTTY TRAINING K943559REMOTE A'LERT K943558PRO'TECT

Related Devices (Code: KPN)

K130951SIMSimavita Pty Limited K971442HUGHES 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 Research K955338DRYTIME FOR POTTY TRAININGHealth Sense Intl., Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.