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FDA 510(k)

DESERET DISPOSABLE PRESSURE TRANSDUCER

K-Number: K841968 · 1984-08-06

ApplicantParke-Davis Co.
Decision Date1984-08-06
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DESERET DISPOSABLE PRESSURE TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Parke-Davis Co.. It received FDA 510(k) clearance on 1984-08-06 under 510(k) number K841968. 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 DESERET DISPOSABLE PRESSURE TRANSDUCER?

DESERET DISPOSABLE PRESSURE TRANSDUCER is a medical device that received FDA 510(k) clearance on 1984-08-06. The listed applicant is Parke-Davis Co.. The 510(k) number is K841968.

When did DESERET DISPOSABLE PRESSURE TRANSDUCER receive FDA 510(k) clearance?

DESERET DISPOSABLE PRESSURE TRANSDUCER received FDA 510(k) clearance on 1984-08-06, under 510(k) number K841968.

Who is the listed applicant for DESERET DISPOSABLE PRESSURE TRANSDUCER?

The FDA 510(k) record lists Parke-Davis Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DESERET DISPOSABLE PRESSURE TRANSDUCER?

The FDA product code for DESERET DISPOSABLE PRESSURE TRANSDUCER is DRS.

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Related Devices (Code: DRS)

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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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