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FDA 510(k)

DETECTOR PAD

K-Number: K782093 · 1979-02-21

ApplicantHalperin Institute, Ltd. The
Decision Date1979-02-21
Product CodeKPN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DETECTOR PAD is the device name listed in this FDA 510(k) record. The listed applicant is Halperin Institute, Ltd. The. It received FDA 510(k) clearance on 1979-02-21 under 510(k) number K782093. 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 DETECTOR PAD?

DETECTOR PAD is a medical device that received FDA 510(k) clearance on 1979-02-21. The listed applicant is Halperin Institute, Ltd. The. The 510(k) number is K782093.

When did DETECTOR PAD receive FDA 510(k) clearance?

DETECTOR PAD received FDA 510(k) clearance on 1979-02-21, under 510(k) number K782093.

Who is the listed applicant for DETECTOR PAD?

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

What is the FDA product code for DETECTOR PAD?

The FDA product code for DETECTOR PAD 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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