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FDA 510(k)

OPTIONAL TOTAL CA-MODULE FOR IL 504/508

K-Number: K812872 · 1981-10-26

ApplicantInstrumentation Laboratory CO
Decision Date1981-10-26
Product CodeCIS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

OPTIONAL TOTAL CA-MODULE FOR IL 504/508 is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory CO. It received FDA 510(k) clearance on 1981-10-26 under 510(k) number K812872. The device is classified under product code CIS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTIONAL TOTAL CA-MODULE FOR IL 504/508?

OPTIONAL TOTAL CA-MODULE FOR IL 504/508 is a medical device that received FDA 510(k) clearance on 1981-10-26. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K812872.

When did OPTIONAL TOTAL CA-MODULE FOR IL 504/508 receive FDA 510(k) clearance?

OPTIONAL TOTAL CA-MODULE FOR IL 504/508 received FDA 510(k) clearance on 1981-10-26, under 510(k) number K812872.

Who is the listed applicant for OPTIONAL TOTAL CA-MODULE FOR IL 504/508?

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

What is the FDA product code for OPTIONAL TOTAL CA-MODULE FOR IL 504/508?

The FDA product code for OPTIONAL TOTAL CA-MODULE FOR IL 504/508 is CIS.

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Related Devices (Code: CIS)

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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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