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FDA 510(k)

ELECTROMEDICS D1079E

K-Number: K873561 · 1987-11-05

ApplicantElectromedics, Inc.
Decision Date1987-11-05
Product CodeDTR
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELECTROMEDICS D1079E is the device name listed in this FDA 510(k) record. The listed applicant is Electromedics, Inc.. It received FDA 510(k) clearance on 1987-11-05 under 510(k) number K873561. The device is classified under product code DTR. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROMEDICS D1079E?

ELECTROMEDICS D1079E is a medical device that received FDA 510(k) clearance on 1987-11-05. The listed applicant is Electromedics, Inc.. The 510(k) number is K873561.

When did ELECTROMEDICS D1079E receive FDA 510(k) clearance?

ELECTROMEDICS D1079E received FDA 510(k) clearance on 1987-11-05, under 510(k) number K873561.

Who is the listed applicant for ELECTROMEDICS D1079E?

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

What is the FDA product code for ELECTROMEDICS D1079E?

The FDA product code for ELECTROMEDICS D1079E is DTR.

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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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