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FDA 510(k)

ELECTRO-ACUSCOPE

K-Number: K832442 · 1983-10-31

ApplicantKenneth J. Purcell
Decision Date1983-10-31
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTRO-ACUSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Kenneth J. Purcell. It received FDA 510(k) clearance on 1983-10-31 under 510(k) number K832442. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRO-ACUSCOPE?

ELECTRO-ACUSCOPE is a medical device that received FDA 510(k) clearance on 1983-10-31. The listed applicant is Kenneth J. Purcell. The 510(k) number is K832442.

When did ELECTRO-ACUSCOPE receive FDA 510(k) clearance?

ELECTRO-ACUSCOPE received FDA 510(k) clearance on 1983-10-31, under 510(k) number K832442.

Who is the listed applicant for ELECTRO-ACUSCOPE?

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

What is the FDA product code for ELECTRO-ACUSCOPE?

The FDA product code for ELECTRO-ACUSCOPE is GZJ.

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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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