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FDA 510(k)

MICROSTREP PLUS PANEL AMOXICILLIN/CLAVULANIC ACID

K-Number: K062596 · 2006-09-19

ApplicantDade Behring, Inc.
Decision Date2006-09-19
Product CodeLRG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MICROSTREP PLUS PANEL AMOXICILLIN/CLAVULANIC ACID is the device name listed in this FDA 510(k) record. The listed applicant is Dade Behring, Inc.. It received FDA 510(k) clearance on 2006-09-19 under 510(k) number K062596. The device is classified under product code LRG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROSTREP PLUS PANEL AMOXICILLIN/CLAVULANIC ACID?

MICROSTREP PLUS PANEL AMOXICILLIN/CLAVULANIC ACID is a medical device that received FDA 510(k) clearance on 2006-09-19. The listed applicant is Dade Behring, Inc.. The 510(k) number is K062596.

When did MICROSTREP PLUS PANEL AMOXICILLIN/CLAVULANIC ACID receive FDA 510(k) clearance?

MICROSTREP PLUS PANEL AMOXICILLIN/CLAVULANIC ACID received FDA 510(k) clearance on 2006-09-19, under 510(k) number K062596.

Who is the listed applicant for MICROSTREP PLUS PANEL AMOXICILLIN/CLAVULANIC ACID?

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

What is the FDA product code for MICROSTREP PLUS PANEL AMOXICILLIN/CLAVULANIC ACID?

The FDA product code for MICROSTREP PLUS PANEL AMOXICILLIN/CLAVULANIC ACID is LRG.

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Related Devices (Code: LRG)

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.

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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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