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FDA 510(k)

BEHRING CHROMOTIMER

K-Number: K901829 · 1990-07-24

ApplicantBehring Diagnostics, Inc.
Decision Date1990-07-24
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BEHRING CHROMOTIMER 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 1990-07-24 under 510(k) number K901829. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEHRING CHROMOTIMER?

BEHRING CHROMOTIMER is a medical device that received FDA 510(k) clearance on 1990-07-24. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K901829.

When did BEHRING CHROMOTIMER receive FDA 510(k) clearance?

BEHRING CHROMOTIMER received FDA 510(k) clearance on 1990-07-24, under 510(k) number K901829.

Who is the listed applicant for BEHRING CHROMOTIMER?

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 CHROMOTIMER?

The FDA product code for BEHRING CHROMOTIMER is JJQ.

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Other records listing Behring Diagnostics, Inc. as applicant

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Related Devices (Code: JJQ)

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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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