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FDA 510(k)

MICROSCAN MICROSTREP PLUS PANEL NEW ANTIMICROBIAL - CEFACLOR

K-Number: K020691 · 2002-04-30

ApplicantDade Microscan, Inc.
Decision Date2002-04-30
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MICROSCAN MICROSTREP PLUS PANEL NEW ANTIMICROBIAL - CEFACLOR is the device name listed in this FDA 510(k) record. The listed applicant is Dade Microscan, Inc.. It received FDA 510(k) clearance on 2002-04-30 under 510(k) number K020691. The device is classified under product code JWY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROSCAN MICROSTREP PLUS PANEL NEW ANTIMICROBIAL - CEFACLOR?

MICROSCAN MICROSTREP PLUS PANEL NEW ANTIMICROBIAL - CEFACLOR is a medical device that received FDA 510(k) clearance on 2002-04-30. The listed applicant is Dade Microscan, Inc.. The 510(k) number is K020691.

When did MICROSCAN MICROSTREP PLUS PANEL NEW ANTIMICROBIAL - CEFACLOR receive FDA 510(k) clearance?

MICROSCAN MICROSTREP PLUS PANEL NEW ANTIMICROBIAL - CEFACLOR received FDA 510(k) clearance on 2002-04-30, under 510(k) number K020691.

Who is the listed applicant for MICROSCAN MICROSTREP PLUS PANEL NEW ANTIMICROBIAL - CEFACLOR?

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

What is the FDA product code for MICROSCAN MICROSTREP PLUS PANEL NEW ANTIMICROBIAL - CEFACLOR?

The FDA product code for MICROSCAN MICROSTREP PLUS PANEL NEW ANTIMICROBIAL - CEFACLOR is JWY.

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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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