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FDA 510(k)

DATA MANAGEMENT SYSTEM IL MODEL 775

K-Number: K800282 · 1980-03-05

ApplicantInstrumentation Laboratory CO
Decision Date1980-03-05
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DATA MANAGEMENT SYSTEM IL MODEL 775 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 1980-03-05 under 510(k) number K800282. The device is classified under product code JQP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DATA MANAGEMENT SYSTEM IL MODEL 775?

DATA MANAGEMENT SYSTEM IL MODEL 775 is a medical device that received FDA 510(k) clearance on 1980-03-05. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K800282.

When did DATA MANAGEMENT SYSTEM IL MODEL 775 receive FDA 510(k) clearance?

DATA MANAGEMENT SYSTEM IL MODEL 775 received FDA 510(k) clearance on 1980-03-05, under 510(k) number K800282.

Who is the listed applicant for DATA MANAGEMENT SYSTEM IL MODEL 775?

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 DATA MANAGEMENT SYSTEM IL MODEL 775?

The FDA product code for DATA MANAGEMENT SYSTEM IL MODEL 775 is JQP.

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Related Devices (Code: JQP)

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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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