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FDA 510(k)

DISPOSABLE PRESSURE TRANSDUCER

K-Number: K830210 · 1983-04-18

ApplicantAmerican Pharmaseal Div. Ahsc
Decision Date1983-04-18
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE PRESSURE TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is American Pharmaseal Div. Ahsc. It received FDA 510(k) clearance on 1983-04-18 under 510(k) number K830210. 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?

DISPOSABLE PRESSURE TRANSDUCER is a medical device that received FDA 510(k) clearance on 1983-04-18. The listed applicant is American Pharmaseal Div. Ahsc. The 510(k) number is K830210.

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

DISPOSABLE PRESSURE TRANSDUCER received FDA 510(k) clearance on 1983-04-18, under 510(k) number K830210.

Who is the listed applicant for DISPOSABLE PRESSURE TRANSDUCER?

The FDA 510(k) record lists American Pharmaseal Div. Ahsc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE PRESSURE TRANSDUCER?

The FDA product code for DISPOSABLE PRESSURE TRANSDUCER is DRS.

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Other records listing American Pharmaseal Div. Ahsc as applicant

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K254074TruPressProcerus EnterprisesK242909FloTrac sensors; FloTrac Jr sensors; Acumen IQ sensors; VolumeView sensorsEdwards Lifesciences, LLCK221782Meritrans ECO Reusable Pressure Transducer, Meritrans ECO DomesMerit Medical Pte. , Ltd.K172458HemoDraw Plus Closed Blood Sampling System with LogiCal Transducer Kit, HemoDraw Plus Closed Blood Sampling System with Transtar Transducer KitSmiths Medical Asd, Inc.K163172HemoDraw Plus Closed Blood Sampling System with LogiCal Transducer Kit, HemoDraw Plus Closed Blood Sampling System with Transtar Transducer KitSmiths Medical Asd, Inc.K161408Compass Cast and MAPCenturion Medical Products Corporation

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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