Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

NEW FREEDOM THIN DEODORANT MAXI PADS

K-Number: K890655 · 1989-05-01

ApplicantKimberly-Clark Corp.
Decision Date1989-05-01
Product CodeHHL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

NEW FREEDOM THIN DEODORANT MAXI PADS is the device name listed in this FDA 510(k) record. The listed applicant is Kimberly-Clark Corp.. It received FDA 510(k) clearance on 1989-05-01 under 510(k) number K890655. The device is classified under product code HHL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEW FREEDOM THIN DEODORANT MAXI PADS?

NEW FREEDOM THIN DEODORANT MAXI PADS is a medical device that received FDA 510(k) clearance on 1989-05-01. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K890655.

When did NEW FREEDOM THIN DEODORANT MAXI PADS receive FDA 510(k) clearance?

NEW FREEDOM THIN DEODORANT MAXI PADS received FDA 510(k) clearance on 1989-05-01, under 510(k) number K890655.

Who is the listed applicant for NEW FREEDOM THIN DEODORANT MAXI PADS?

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

What is the FDA product code for NEW FREEDOM THIN DEODORANT MAXI PADS?

The FDA product code for NEW FREEDOM THIN DEODORANT MAXI PADS is HHL.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Kimberly-Clark Corp. 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.

K131879KC 300 SURGICAL MASKK131841KIMBERLY-CLARK LAVENDER NITRILE POWDER-FREE EXAM GLOVEK131254KIMVENT MICROCUFF SUBGLOTTIC SUCTIONING ENDOTRACHEAL TUBEK120985KIMVENT MICROCUFF SUBGLOTTIC SUCTIONINGK112805KIMGUARD ONE-STEP STERILIZATION WRAPK113423KIMBERLY CLARK PURPLE NITRILE, AND PURPLE NITRILE XTRA POWDER FREE EXAM GLOVE

View all 102 devices →

Related Devices (Code: HHL)

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.

K962954DEODORANT MAXI PADParagon Trade Brands, Inc.K962953DEODORANT PANTY SHIELDParagon Trade Brands, Inc.K962962DEODORANT PANTY LINERParagon Trade Brands, Inc.K961119CAREFREE PANTYLINERSPersonal Products Co.K913237ALWAYS, SCENTED/SCENTED DEODORIZED MENSTRUAL PADProcter & Gamble Co.K913238ALWAYS, UNSCENTED MENSTRUAL PADProcter & Gamble Co.

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.

↑