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FDA 510(k)

HEXIDIS ALCOHOL SWAB

K-Number: K910735 · 1991-04-02

ApplicantSpecialites Septodont
Decision Date1991-04-02
Product CodeLKB
DecisionSubstantially Equivalent

Device Summary

HEXIDIS ALCOHOL SWAB is the device name listed in this FDA 510(k) record. The listed applicant is Specialites Septodont. It received FDA 510(k) clearance on 1991-04-02 under 510(k) number K910735. The device is classified under product code LKB. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEXIDIS ALCOHOL SWAB?

HEXIDIS ALCOHOL SWAB is a medical device that received FDA 510(k) clearance on 1991-04-02. The listed applicant is Specialites Septodont. The 510(k) number is K910735.

When did HEXIDIS ALCOHOL SWAB receive FDA 510(k) clearance?

HEXIDIS ALCOHOL SWAB received FDA 510(k) clearance on 1991-04-02, under 510(k) number K910735.

Who is the listed applicant for HEXIDIS ALCOHOL SWAB?

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

What is the FDA product code for HEXIDIS ALCOHOL SWAB?

The FDA product code for HEXIDIS ALCOHOL SWAB is LKB.

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Other records listing Specialites Septodont 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.

K012427PHARMAETHYL LOCAL PULP AND VITALITY TESTING AGENTK010415ISODANK982773QUICKSET LIQUID AND POWDERK982671SECURALLOYK980633ENDOSOLV EK920692SEPTOCALCINE ULTRA

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Related Devices (Code: LKB)

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.

K121655BD ALCOHOL SWABBecton, Dickinson & COK112791SITESCRUB IPA DEVICEC. R. BardK912161I.V. STARR KITMedical Device Inspection Co., Inc.K912731STERI-SWABWestlock Investments (Usa), Inc.K896898BOWEN ELECTRODE SKIN PREPATORY CLEANSERBowen & Company, Inc.K896835ALCOHOL PREP AND POVIDONE-IODINE PREPNorpak Mfg., 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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