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FDA 510(k)

ACUPRESS VIBRATOR

K-Number: K812902 · 1981-11-10

ApplicantEicona Corp.
Decision Date1981-11-10
Product CodeIRO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ACUPRESS VIBRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Eicona Corp.. It received FDA 510(k) clearance on 1981-11-10 under 510(k) number K812902. 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 ACUPRESS VIBRATOR?

ACUPRESS VIBRATOR is a medical device that received FDA 510(k) clearance on 1981-11-10. The listed applicant is Eicona Corp.. The 510(k) number is K812902.

When did ACUPRESS VIBRATOR receive FDA 510(k) clearance?

ACUPRESS VIBRATOR received FDA 510(k) clearance on 1981-11-10, under 510(k) number K812902.

Who is the listed applicant for ACUPRESS VIBRATOR?

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

What is the FDA product code for ACUPRESS VIBRATOR?

The FDA product code for ACUPRESS VIBRATOR 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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