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FDA 510(k)

FISHER-PRICE DRY NIGHT MONITOR

K-Number: K942057 · 1994-07-28

ApplicantFisher Price
Decision Date1994-07-28
Product CodeKPN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FISHER-PRICE DRY NIGHT MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Fisher Price. It received FDA 510(k) clearance on 1994-07-28 under 510(k) number K942057. 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 FISHER-PRICE DRY NIGHT MONITOR?

FISHER-PRICE DRY NIGHT MONITOR is a medical device that received FDA 510(k) clearance on 1994-07-28. The listed applicant is Fisher Price. The 510(k) number is K942057.

When did FISHER-PRICE DRY NIGHT MONITOR receive FDA 510(k) clearance?

FISHER-PRICE DRY NIGHT MONITOR received FDA 510(k) clearance on 1994-07-28, under 510(k) number K942057.

Who is the listed applicant for FISHER-PRICE DRY NIGHT MONITOR?

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

What is the FDA product code for FISHER-PRICE DRY NIGHT MONITOR?

The FDA product code for FISHER-PRICE DRY NIGHT 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.

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Other records listing Fisher Price 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.

K864399FISHER PRICE SUNJAMMERS

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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