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FDA 510(k)

PRINTER, IL 460

K-Number: K760232 · 1976-08-26

ApplicantInstrumentation Laboratory CO
Decision Date1976-08-26
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PRINTER, IL 460 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 1976-08-26 under 510(k) number K760232. 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 PRINTER, IL 460?

PRINTER, IL 460 is a medical device that received FDA 510(k) clearance on 1976-08-26. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K760232.

When did PRINTER, IL 460 receive FDA 510(k) clearance?

PRINTER, IL 460 received FDA 510(k) clearance on 1976-08-26, under 510(k) number K760232.

Who is the listed applicant for PRINTER, IL 460?

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 PRINTER, IL 460?

The FDA product code for PRINTER, IL 460 is 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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