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FDA 510(k)

CHLAMYDIAZYME/COMMANDER INSTRUMENTATION

K-Number: K885006 · 1988-12-16

ApplicantAbbott Laboratories
Decision Date1988-12-16
Product CodeLJC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CHLAMYDIAZYME/COMMANDER INSTRUMENTATION is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1988-12-16 under 510(k) number K885006. The device is classified under product code LJC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHLAMYDIAZYME/COMMANDER INSTRUMENTATION?

CHLAMYDIAZYME/COMMANDER INSTRUMENTATION is a medical device that received FDA 510(k) clearance on 1988-12-16. The listed applicant is Abbott Laboratories. The 510(k) number is K885006.

When did CHLAMYDIAZYME/COMMANDER INSTRUMENTATION receive FDA 510(k) clearance?

CHLAMYDIAZYME/COMMANDER INSTRUMENTATION received FDA 510(k) clearance on 1988-12-16, under 510(k) number K885006.

Who is the listed applicant for CHLAMYDIAZYME/COMMANDER INSTRUMENTATION?

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

What is the FDA product code for CHLAMYDIAZYME/COMMANDER INSTRUMENTATION?

The FDA product code for CHLAMYDIAZYME/COMMANDER INSTRUMENTATION is LJC.

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Related Devices (Code: LJC)

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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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