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FDA 510(k)

PHYSIOLOGICAL PRESSURE TRANSDUCER 1290A

K-Number: K771361 · 1977-08-04

ApplicantHewlett-Packard Co.
Decision Date1977-08-04
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PHYSIOLOGICAL PRESSURE TRANSDUCER 1290A is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1977-08-04 under 510(k) number K771361. 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 1290A?

PHYSIOLOGICAL PRESSURE TRANSDUCER 1290A is a medical device that received FDA 510(k) clearance on 1977-08-04. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K771361.

When did PHYSIOLOGICAL PRESSURE TRANSDUCER 1290A receive FDA 510(k) clearance?

PHYSIOLOGICAL PRESSURE TRANSDUCER 1290A received FDA 510(k) clearance on 1977-08-04, under 510(k) number K771361.

Who is the listed applicant for PHYSIOLOGICAL PRESSURE TRANSDUCER 1290A?

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

What is the FDA product code for PHYSIOLOGICAL PRESSURE TRANSDUCER 1290A?

The FDA product code for PHYSIOLOGICAL PRESSURE TRANSDUCER 1290A 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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