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FDA 510(k)

TRANTEC PHYSIOLOGICAL PRESSURE TRANSDUC

K-Number: K840023 · 1984-06-22

ApplicantAmerican Bentley
Decision Date1984-06-22
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TRANTEC PHYSIOLOGICAL PRESSURE TRANSDUC is the device name listed in this FDA 510(k) record. The listed applicant is American Bentley. It received FDA 510(k) clearance on 1984-06-22 under 510(k) number K840023. 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 TRANTEC PHYSIOLOGICAL PRESSURE TRANSDUC?

TRANTEC PHYSIOLOGICAL PRESSURE TRANSDUC is a medical device that received FDA 510(k) clearance on 1984-06-22. The listed applicant is American Bentley. The 510(k) number is K840023.

When did TRANTEC PHYSIOLOGICAL PRESSURE TRANSDUC receive FDA 510(k) clearance?

TRANTEC PHYSIOLOGICAL PRESSURE TRANSDUC received FDA 510(k) clearance on 1984-06-22, under 510(k) number K840023.

Who is the listed applicant for TRANTEC PHYSIOLOGICAL PRESSURE TRANSDUC?

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

What is the FDA product code for TRANTEC PHYSIOLOGICAL PRESSURE TRANSDUC?

The FDA product code for TRANTEC PHYSIOLOGICAL PRESSURE TRANSDUC is 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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