FDA 510(k)

BEHRING ELISA PROCESSOR M

K-Number: K841043 · 1984-07-06

Decision Date1984-07-06

Product CodeJQW

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

BEHRING ELISA PROCESSOR M is the device name listed in this FDA 510(k) record. The listed applicant is Behring Diagnostics, Inc.. It received FDA 510(k) clearance on 1984-07-06 under 510(k) number K841043. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEHRING ELISA PROCESSOR M?

BEHRING ELISA PROCESSOR M is a medical device that received FDA 510(k) clearance on 1984-07-06. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K841043.

When did BEHRING ELISA PROCESSOR M receive FDA 510(k) clearance?

BEHRING ELISA PROCESSOR M received FDA 510(k) clearance on 1984-07-06, under 510(k) number K841043.

Who is the listed applicant for BEHRING ELISA PROCESSOR M?

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

What is the FDA product code for BEHRING ELISA PROCESSOR M?

The FDA product code for BEHRING ELISA PROCESSOR M is JQW.

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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.