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FDA 510(k)

BOWEN ELECTRODE SKIN PREPATORY CLEANSER

K-Number: K896898 · 1990-04-04

ApplicantBowen & Company, Inc.
Decision Date1990-04-04
Product CodeLKB
DecisionSubstantially Equivalent

Device Summary

BOWEN ELECTRODE SKIN PREPATORY CLEANSER is the device name listed in this FDA 510(k) record. The listed applicant is Bowen & Company, Inc.. It received FDA 510(k) clearance on 1990-04-04 under 510(k) number K896898. The device is classified under product code LKB. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOWEN ELECTRODE SKIN PREPATORY CLEANSER?

BOWEN ELECTRODE SKIN PREPATORY CLEANSER is a medical device that received FDA 510(k) clearance on 1990-04-04. The listed applicant is Bowen & Company, Inc.. The 510(k) number is K896898.

When did BOWEN ELECTRODE SKIN PREPATORY CLEANSER receive FDA 510(k) clearance?

BOWEN ELECTRODE SKIN PREPATORY CLEANSER received FDA 510(k) clearance on 1990-04-04, under 510(k) number K896898.

Who is the listed applicant for BOWEN ELECTRODE SKIN PREPATORY CLEANSER?

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

What is the FDA product code for BOWEN ELECTRODE SKIN PREPATORY CLEANSER?

The FDA product code for BOWEN ELECTRODE SKIN PREPATORY CLEANSER is LKB.

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Other records listing Bowen & Company, 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.

K896538DISPOSABLE 45 DEGREE SHAVERK873766STERNAL POWER AWLK872098CREMEEN ALVEOLAR BONE CALIPERK871325BOWEN REUSEABLE/DISPOSABLE ELECTRODEK87088245 DEGREE SHAVERK870881LOOSE BODY GRASPERS

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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 SeptodontK896835ALCOHOL 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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