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FDA 510(k)

PHYSIOLOGICAL PRESSURE TRANSDUCER #900

K-Number: K820342 · 1982-03-04

ApplicantBentley Laboratories, Inc.
Decision Date1982-03-04
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PHYSIOLOGICAL PRESSURE TRANSDUCER #900 is the device name listed in this FDA 510(k) record. The listed applicant is Bentley Laboratories, Inc.. It received FDA 510(k) clearance on 1982-03-04 under 510(k) number K820342. 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 PHYSIOLOGICAL PRESSURE TRANSDUCER #900?

PHYSIOLOGICAL PRESSURE TRANSDUCER #900 is a medical device that received FDA 510(k) clearance on 1982-03-04. The listed applicant is Bentley Laboratories, Inc.. The 510(k) number is K820342.

When did PHYSIOLOGICAL PRESSURE TRANSDUCER #900 receive FDA 510(k) clearance?

PHYSIOLOGICAL PRESSURE TRANSDUCER #900 received FDA 510(k) clearance on 1982-03-04, under 510(k) number K820342.

Who is the listed applicant for PHYSIOLOGICAL PRESSURE TRANSDUCER #900?

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

What is the FDA product code for PHYSIOLOGICAL PRESSURE TRANSDUCER #900?

The FDA product code for PHYSIOLOGICAL PRESSURE TRANSDUCER #900 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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