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FDA 510(k)

25-50 EKG RULER

K-Number: K790691 · 1979-04-16

ApplicantMedical Engineering Designs Co., Inc.
Decision Date1979-04-16
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

25-50 EKG RULER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Engineering Designs Co., Inc.. It received FDA 510(k) clearance on 1979-04-16 under 510(k) number K790691. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 25-50 EKG RULER?

25-50 EKG RULER is a medical device that received FDA 510(k) clearance on 1979-04-16. The listed applicant is Medical Engineering Designs Co., Inc.. The 510(k) number is K790691.

When did 25-50 EKG RULER receive FDA 510(k) clearance?

25-50 EKG RULER received FDA 510(k) clearance on 1979-04-16, under 510(k) number K790691.

Who is the listed applicant for 25-50 EKG RULER?

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

What is the FDA product code for 25-50 EKG RULER?

The FDA product code for 25-50 EKG RULER is DPS.

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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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