FDA 510(k)

DR. DRY

K-Number: K895346 · 1989-10-24

Decision Date1989-10-24

Product CodeKPN

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

DR. DRY is the device name listed in this FDA 510(k) record. The listed applicant is Intellitech. It received FDA 510(k) clearance on 1989-10-24 under 510(k) number K895346. 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 DR. DRY?

DR. DRY is a medical device that received FDA 510(k) clearance on 1989-10-24. The listed applicant is Intellitech. The 510(k) number is K895346.

When did DR. DRY receive FDA 510(k) clearance?

DR. DRY received FDA 510(k) clearance on 1989-10-24, under 510(k) number K895346.

Who is the listed applicant for DR. DRY?

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

What is the FDA product code for DR. DRY?

The FDA product code for DR. DRY is KPN.

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 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

View on FDA Database →

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