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FDA 510(k)

ARTIMICROBIAL REMOVAL DEVICE

K-Number: K830372 · 1983-04-08

ApplicantMarion Laboratories, Inc.
Decision Date1983-04-08
Product CodeLJF
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ARTIMICROBIAL REMOVAL DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Marion Laboratories, Inc.. It received FDA 510(k) clearance on 1983-04-08 under 510(k) number K830372. The device is classified under product code LJF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTIMICROBIAL REMOVAL DEVICE?

ARTIMICROBIAL REMOVAL DEVICE is a medical device that received FDA 510(k) clearance on 1983-04-08. The listed applicant is Marion Laboratories, Inc.. The 510(k) number is K830372.

When did ARTIMICROBIAL REMOVAL DEVICE receive FDA 510(k) clearance?

ARTIMICROBIAL REMOVAL DEVICE received FDA 510(k) clearance on 1983-04-08, under 510(k) number K830372.

Who is the listed applicant for ARTIMICROBIAL REMOVAL DEVICE?

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

What is the FDA product code for ARTIMICROBIAL REMOVAL DEVICE?

The FDA product code for ARTIMICROBIAL REMOVAL DEVICE is LJF.

Related Clinical Trials

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Other records listing Marion Laboratories, 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.

K883391POLYMER ADHESIVE BANDAGEK875182MODIFIED LABELING FOR TOXI-LAB THC SCREENK875181MODIFIED LABELING FOR TOXI-LAB BROAD SPECTRUMK874554ENVICLUSIVE (TM)K874552ENVISAN PADK874551ENVINET(TM)

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Related Devices (Code: LJF)

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.

K003104BACT/ALERT CSROrganon Teknika Corp.K830363BACTEC 170 TRYPTIC SOY BROTH W/RESINSBd Becton Dickinson Vacutainer Systems PreanalyticK822344ANTIMICROBIAL REMOVAL DEVICE (ARD)Marion Laboratories, 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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