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FDA 510(k)

DISPOSABLE BLOOD PRESSURE TRANSDUCER

K-Number: K821416 · 1982-07-02

ApplicantBentley Laboratories, Inc.
Decision Date1982-07-02
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE BLOOD PRESSURE TRANSDUCER 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 1982-07-02 under 510(k) number K821416. 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 DISPOSABLE BLOOD PRESSURE TRANSDUCER?

DISPOSABLE BLOOD PRESSURE TRANSDUCER is a medical device that received FDA 510(k) clearance on 1982-07-02. The listed applicant is Bentley Laboratories, Inc.. The 510(k) number is K821416.

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

DISPOSABLE BLOOD PRESSURE TRANSDUCER received FDA 510(k) clearance on 1982-07-02, under 510(k) number K821416.

Who is the listed applicant for DISPOSABLE BLOOD PRESSURE TRANSDUCER?

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 DISPOSABLE BLOOD PRESSURE TRANSDUCER?

The FDA product code for DISPOSABLE BLOOD PRESSURE TRANSDUCER 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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