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FDA 510(k)

ELECTRO-ACUSCOPE-70

K-Number: K801459 · 1980-08-20

ApplicantNebrensky Corp.
Decision Date1980-08-20
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTRO-ACUSCOPE-70 is the device name listed in this FDA 510(k) record. The listed applicant is Nebrensky Corp.. It received FDA 510(k) clearance on 1980-08-20 under 510(k) number K801459. 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-70?

ELECTRO-ACUSCOPE-70 is a medical device that received FDA 510(k) clearance on 1980-08-20. The listed applicant is Nebrensky Corp.. The 510(k) number is K801459.

When did ELECTRO-ACUSCOPE-70 receive FDA 510(k) clearance?

ELECTRO-ACUSCOPE-70 received FDA 510(k) clearance on 1980-08-20, under 510(k) number K801459.

Who is the listed applicant for ELECTRO-ACUSCOPE-70?

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

What is the FDA product code for ELECTRO-ACUSCOPE-70?

The FDA product code for ELECTRO-ACUSCOPE-70 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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