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FDA 510(k)

DOCUMENTOR

K-Number: K842715 · 1984-11-19

ApplicantLife Technology
Decision Date1984-11-19
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DOCUMENTOR is the device name listed in this FDA 510(k) record. The listed applicant is Life Technology. It received FDA 510(k) clearance on 1984-11-19 under 510(k) number K842715. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOCUMENTOR?

DOCUMENTOR is a medical device that received FDA 510(k) clearance on 1984-11-19. The listed applicant is Life Technology. The 510(k) number is K842715.

When did DOCUMENTOR receive FDA 510(k) clearance?

DOCUMENTOR received FDA 510(k) clearance on 1984-11-19, under 510(k) number K842715.

Who is the listed applicant for DOCUMENTOR?

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

What is the FDA product code for DOCUMENTOR?

The FDA product code for DOCUMENTOR is DSI.

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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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