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FDA 510(k)

DRY COMFORT DISPOSABLE UNDERPAD

K-Number: K881969 · 1988-06-07

Decision Date1988-06-07
Product CodeKME
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DRY COMFORT DISPOSABLE UNDERPAD is the device name listed in this FDA 510(k) record. The listed applicant is Health Tec, Inc.. It received FDA 510(k) clearance on 1988-06-07 under 510(k) number K881969. The device is classified under product code KME. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRY COMFORT DISPOSABLE UNDERPAD?

DRY COMFORT DISPOSABLE UNDERPAD is a medical device that received FDA 510(k) clearance on 1988-06-07. The listed applicant is Health Tec, Inc.. The 510(k) number is K881969.

When did DRY COMFORT DISPOSABLE UNDERPAD receive FDA 510(k) clearance?

DRY COMFORT DISPOSABLE UNDERPAD received FDA 510(k) clearance on 1988-06-07, under 510(k) number K881969.

Who is the listed applicant for DRY COMFORT DISPOSABLE UNDERPAD?

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

What is the FDA product code for DRY COMFORT DISPOSABLE UNDERPAD?

The FDA product code for DRY COMFORT DISPOSABLE UNDERPAD is KME.

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.

Other records listing Health Tec, 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.

Related Devices (Code: KME)

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.

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.

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