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FDA 510(k)

MEDICAL OSCILLOSCOPE MEMORY SCOPE

K-Number: K760721 · 1976-10-06

ApplicantAbbott Laboratories
Decision Date1976-10-06
Product CodeDXJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDICAL OSCILLOSCOPE MEMORY SCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1976-10-06 under 510(k) number K760721. The device is classified under product code DXJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICAL OSCILLOSCOPE MEMORY SCOPE?

MEDICAL OSCILLOSCOPE MEMORY SCOPE is a medical device that received FDA 510(k) clearance on 1976-10-06. The listed applicant is Abbott Laboratories. The 510(k) number is K760721.

When did MEDICAL OSCILLOSCOPE MEMORY SCOPE receive FDA 510(k) clearance?

MEDICAL OSCILLOSCOPE MEMORY SCOPE received FDA 510(k) clearance on 1976-10-06, under 510(k) number K760721.

Who is the listed applicant for MEDICAL OSCILLOSCOPE MEMORY SCOPE?

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

What is the FDA product code for MEDICAL OSCILLOSCOPE MEMORY SCOPE?

The FDA product code for MEDICAL OSCILLOSCOPE MEMORY SCOPE is DXJ.

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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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