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FDA 510(k)

PRESSURE TRANSDUCER AIRFLOW SENSOR

K-Number: K982293 · 1998-07-13

Decision Date1998-07-13
Product CodeMNR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PRESSURE TRANSDUCER AIRFLOW SENSOR is the device name listed in this FDA 510(k) record. The listed applicant is Pro-Tech Services, Inc.. It received FDA 510(k) clearance on 1998-07-13 under 510(k) number K982293. The device is classified under product code MNR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESSURE TRANSDUCER AIRFLOW SENSOR?

PRESSURE TRANSDUCER AIRFLOW SENSOR is a medical device that received FDA 510(k) clearance on 1998-07-13. The listed applicant is Pro-Tech Services, Inc.. The 510(k) number is K982293.

When did PRESSURE TRANSDUCER AIRFLOW SENSOR receive FDA 510(k) clearance?

PRESSURE TRANSDUCER AIRFLOW SENSOR received FDA 510(k) clearance on 1998-07-13, under 510(k) number K982293.

Who is the listed applicant for PRESSURE TRANSDUCER AIRFLOW SENSOR?

The FDA 510(k) record lists Pro-Tech Services, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRESSURE TRANSDUCER AIRFLOW SENSOR?

The FDA product code for PRESSURE TRANSDUCER AIRFLOW SENSOR is MNR.

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 Pro-Tech Services, 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: MNR)

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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