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FDA 510(k)

SINGLE CHANNEL NONFADE OSCILLOSCOPE

K-Number: K822517 · 1982-09-14

ApplicantQuinton, Inc.
Decision Date1982-09-14
Product CodeDXJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SINGLE CHANNEL NONFADE OSCILLOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1982-09-14 under 510(k) number K822517. 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 SINGLE CHANNEL NONFADE OSCILLOSCOPE?

SINGLE CHANNEL NONFADE OSCILLOSCOPE is a medical device that received FDA 510(k) clearance on 1982-09-14. The listed applicant is Quinton, Inc.. The 510(k) number is K822517.

When did SINGLE CHANNEL NONFADE OSCILLOSCOPE receive FDA 510(k) clearance?

SINGLE CHANNEL NONFADE OSCILLOSCOPE received FDA 510(k) clearance on 1982-09-14, under 510(k) number K822517.

Who is the listed applicant for SINGLE CHANNEL NONFADE OSCILLOSCOPE?

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

What is the FDA product code for SINGLE CHANNEL NONFADE OSCILLOSCOPE?

The FDA product code for SINGLE CHANNEL NONFADE OSCILLOSCOPE is DXJ.

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Related Devices (Code: 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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