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FDA 510(k)

QUICKPAD (ALCOHOL SWABS)

K-Number: K892193 · 1989-08-04

ApplicantHoltsch Co., Inc.
Decision Date1989-08-04
Product CodeLKB
DecisionSubstantially Equivalent

Device Summary

QUICKPAD (ALCOHOL SWABS) is the device name listed in this FDA 510(k) record. The listed applicant is Holtsch Co., Inc.. It received FDA 510(k) clearance on 1989-08-04 under 510(k) number K892193. The device is classified under product code LKB. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICKPAD (ALCOHOL SWABS)?

QUICKPAD (ALCOHOL SWABS) is a medical device that received FDA 510(k) clearance on 1989-08-04. The listed applicant is Holtsch Co., Inc.. The 510(k) number is K892193.

When did QUICKPAD (ALCOHOL SWABS) receive FDA 510(k) clearance?

QUICKPAD (ALCOHOL SWABS) received FDA 510(k) clearance on 1989-08-04, under 510(k) number K892193.

Who is the listed applicant for QUICKPAD (ALCOHOL SWABS)?

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

What is the FDA product code for QUICKPAD (ALCOHOL SWABS)?

The FDA product code for QUICKPAD (ALCOHOL SWABS) is LKB.

Related Clinical Trials

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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.K910735HEXIDIS ALCOHOL SWABSpecialites SeptodontK896898BOWEN ELECTRODE SKIN PREPATORY CLEANSERBowen & Company, 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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