FDA 510(k)

DIGILOG SYSTEM

K-Number: K820958 · 1982-05-13

ApplicantMedical Design Laboratories, Inc.

Decision Date1982-05-13

Product Code

DecisionSubstantially Equivalent

Device Summary

DIGILOG SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medical Design Laboratories, Inc.. It received FDA 510(k) clearance on 1982-05-13 under 510(k) number K820958. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGILOG SYSTEM?

DIGILOG SYSTEM is a medical device that received FDA 510(k) clearance on 1982-05-13. The listed applicant is Medical Design Laboratories, Inc.. The 510(k) number is K820958.

When did DIGILOG SYSTEM receive FDA 510(k) clearance?

DIGILOG SYSTEM received FDA 510(k) clearance on 1982-05-13, under 510(k) number K820958.

Who is the listed applicant for DIGILOG SYSTEM?

The FDA 510(k) record lists Medical Design Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

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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.