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FDA 510(k)

MEDI-TRACE TRANSDUCERS/PHYSIOLOG. MONITO

K-Number: K800705 · 1980-04-16

ApplicantGraphic Controls Corp.
Decision Date1980-04-16
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDI-TRACE TRANSDUCERS/PHYSIOLOG. MONITO is the device name listed in this FDA 510(k) record. The listed applicant is Graphic Controls Corp.. It received FDA 510(k) clearance on 1980-04-16 under 510(k) number K800705. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDI-TRACE TRANSDUCERS/PHYSIOLOG. MONITO?

MEDI-TRACE TRANSDUCERS/PHYSIOLOG. MONITO is a medical device that received FDA 510(k) clearance on 1980-04-16. The listed applicant is Graphic Controls Corp.. The 510(k) number is K800705.

When did MEDI-TRACE TRANSDUCERS/PHYSIOLOG. MONITO receive FDA 510(k) clearance?

MEDI-TRACE TRANSDUCERS/PHYSIOLOG. MONITO received FDA 510(k) clearance on 1980-04-16, under 510(k) number K800705.

Who is the listed applicant for MEDI-TRACE TRANSDUCERS/PHYSIOLOG. MONITO?

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

What is the FDA product code for MEDI-TRACE TRANSDUCERS/PHYSIOLOG. MONITO?

The FDA product code for MEDI-TRACE TRANSDUCERS/PHYSIOLOG. MONITO is DRS.

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Other records listing Graphic Controls Corp. as applicant

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Related Devices (Code: DRS)

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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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