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FDA 510(k)

COMPUTER INTERFACE IL 814

K-Number: K781173 · 1978-09-14

Decision Date1978-09-14
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

COMPUTER INTERFACE IL 814 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 1978-09-14 under 510(k) number K781173. 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 COMPUTER INTERFACE IL 814?

COMPUTER INTERFACE IL 814 is a medical device that received FDA 510(k) clearance on 1978-09-14. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K781173.

When did COMPUTER INTERFACE IL 814 receive FDA 510(k) clearance?

COMPUTER INTERFACE IL 814 received FDA 510(k) clearance on 1978-09-14, under 510(k) number K781173.

Who is the listed applicant for COMPUTER INTERFACE IL 814?

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 COMPUTER INTERFACE IL 814?

The FDA product code for COMPUTER INTERFACE IL 814 is JQP.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Instrumentation Laboratory CO as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: JQP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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