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FDA 510(k)

ELECTRICAL VIBRATING DEVICE

K-Number: K821133 · 1982-07-09

ApplicantDurham Electric Co.
Decision Date1982-07-09
Product CodeIRO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ELECTRICAL VIBRATING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Durham Electric Co.. It received FDA 510(k) clearance on 1982-07-09 under 510(k) number K821133. The device is classified under product code IRO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRICAL VIBRATING DEVICE?

ELECTRICAL VIBRATING DEVICE is a medical device that received FDA 510(k) clearance on 1982-07-09. The listed applicant is Durham Electric Co.. The 510(k) number is K821133.

When did ELECTRICAL VIBRATING DEVICE receive FDA 510(k) clearance?

ELECTRICAL VIBRATING DEVICE received FDA 510(k) clearance on 1982-07-09, under 510(k) number K821133.

Who is the listed applicant for ELECTRICAL VIBRATING DEVICE?

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

What is the FDA product code for ELECTRICAL VIBRATING DEVICE?

The FDA product code for ELECTRICAL VIBRATING DEVICE is IRO.

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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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