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FDA 510(k)

MODEL:TA-ROSE RESONANT OVERSHOOT ELIMINATOR

K-Number: K855145 · 1986-02-26

ApplicantGould, Inc.
Decision Date1986-02-26
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL:TA-ROSE RESONANT OVERSHOOT ELIMINATOR is the device name listed in this FDA 510(k) record. The listed applicant is Gould, Inc.. It received FDA 510(k) clearance on 1986-02-26 under 510(k) number K855145. 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 MODEL:TA-ROSE RESONANT OVERSHOOT ELIMINATOR?

MODEL:TA-ROSE RESONANT OVERSHOOT ELIMINATOR is a medical device that received FDA 510(k) clearance on 1986-02-26. The listed applicant is Gould, Inc.. The 510(k) number is K855145.

When did MODEL:TA-ROSE RESONANT OVERSHOOT ELIMINATOR receive FDA 510(k) clearance?

MODEL:TA-ROSE RESONANT OVERSHOOT ELIMINATOR received FDA 510(k) clearance on 1986-02-26, under 510(k) number K855145.

Who is the listed applicant for MODEL:TA-ROSE RESONANT OVERSHOOT ELIMINATOR?

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

What is the FDA product code for MODEL:TA-ROSE RESONANT OVERSHOOT ELIMINATOR?

The FDA product code for MODEL:TA-ROSE RESONANT OVERSHOOT ELIMINATOR is DRS.

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Other records listing Gould, 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.

K911935CARDIAC ELECTROPHYSICAL LEAD SELECTOR, MODIFIEDK861092MODEL SP1465 CARDIAC OUTPUT COMPUTERK860805PRESSURE MONITOR CATH MODELS SP5325,SP5327,SP5337K854403MODEL 2120 SPIROSCREENK851486GOULD DISPOSABLE TRANSDUCER & ACCESSORIES-DTXK850114C/PES 9201, ECG STRESS TESTING SYS

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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.

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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