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FDA 510(k)

DISPOSABLE PRESSURE TRANSDUCER SYSTEM STERILE

K-Number: K853996 · 1986-05-07

Decision Date1986-05-07
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE PRESSURE TRANSDUCER SYSTEM STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Transamerica Delaval, Inc.. It received FDA 510(k) clearance on 1986-05-07 under 510(k) number K853996. 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 PRESSURE TRANSDUCER SYSTEM STERILE?

DISPOSABLE PRESSURE TRANSDUCER SYSTEM STERILE is a medical device that received FDA 510(k) clearance on 1986-05-07. The listed applicant is Transamerica Delaval, Inc.. The 510(k) number is K853996.

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

DISPOSABLE PRESSURE TRANSDUCER SYSTEM STERILE received FDA 510(k) clearance on 1986-05-07, under 510(k) number K853996.

Who is the listed applicant for DISPOSABLE PRESSURE TRANSDUCER SYSTEM STERILE?

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

What is the FDA product code for DISPOSABLE PRESSURE TRANSDUCER SYSTEM STERILE?

The FDA product code for DISPOSABLE PRESSURE TRANSDUCER SYSTEM STERILE is DRS.

Related Clinical Trials

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.

Other records listing Transamerica Delaval, Inc. as applicant

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.

View all 7 devices →

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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