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FDA 510(k)

DOCUMENT LINEARITY TEST STANDARDS

K-Number: K813411 · 1981-12-18

ApplicantNorth American Standards
Decision Date1981-12-18
Product CodeJIX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DOCUMENT LINEARITY TEST STANDARDS is the device name listed in this FDA 510(k) record. The listed applicant is North American Standards. It received FDA 510(k) clearance on 1981-12-18 under 510(k) number K813411. The device is classified under product code JIX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOCUMENT LINEARITY TEST STANDARDS?

DOCUMENT LINEARITY TEST STANDARDS is a medical device that received FDA 510(k) clearance on 1981-12-18. The listed applicant is North American Standards. The 510(k) number is K813411.

When did DOCUMENT LINEARITY TEST STANDARDS receive FDA 510(k) clearance?

DOCUMENT LINEARITY TEST STANDARDS received FDA 510(k) clearance on 1981-12-18, under 510(k) number K813411.

Who is the listed applicant for DOCUMENT LINEARITY TEST STANDARDS?

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

What is the FDA product code for DOCUMENT LINEARITY TEST STANDARDS?

The FDA product code for DOCUMENT LINEARITY TEST STANDARDS is JIX.

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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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