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FDA 510(k)

DISPOSABLE BLOOD PRESSURE TRANSDUCER DOM

K-Number: K813053 · 1981-11-16

ApplicantBentley Laboratories, Inc.
Decision Date1981-11-16
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE BLOOD PRESSURE TRANSDUCER DOM 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 1981-11-16 under 510(k) number K813053. 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 DOM?

DISPOSABLE BLOOD PRESSURE TRANSDUCER DOM is a medical device that received FDA 510(k) clearance on 1981-11-16. The listed applicant is Bentley Laboratories, Inc.. The 510(k) number is K813053.

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

DISPOSABLE BLOOD PRESSURE TRANSDUCER DOM received FDA 510(k) clearance on 1981-11-16, under 510(k) number K813053.

Who is the listed applicant for DISPOSABLE BLOOD PRESSURE TRANSDUCER DOM?

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 DOM?

The FDA product code for DISPOSABLE BLOOD PRESSURE TRANSDUCER DOM is DRS.

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Related Devices (Code: DRS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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