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FDA 510(k)

OSCILLOMETRIC PULSE DETECTION DEVICE

K-Number: K902453 · 1990-08-23

ApplicantThomas J. Fogarty, M.D.
Decision Date1990-08-23
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

OSCILLOMETRIC PULSE DETECTION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Thomas J. Fogarty, M.D.. It received FDA 510(k) clearance on 1990-08-23 under 510(k) number K902453. 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 OSCILLOMETRIC PULSE DETECTION DEVICE?

OSCILLOMETRIC PULSE DETECTION DEVICE is a medical device that received FDA 510(k) clearance on 1990-08-23. The listed applicant is Thomas J. Fogarty, M.D.. The 510(k) number is K902453.

When did OSCILLOMETRIC PULSE DETECTION DEVICE receive FDA 510(k) clearance?

OSCILLOMETRIC PULSE DETECTION DEVICE received FDA 510(k) clearance on 1990-08-23, under 510(k) number K902453.

Who is the listed applicant for OSCILLOMETRIC PULSE DETECTION DEVICE?

The FDA 510(k) record lists Thomas J. Fogarty, M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OSCILLOMETRIC PULSE DETECTION DEVICE?

The FDA product code for OSCILLOMETRIC PULSE DETECTION DEVICE is DRS.

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Other records listing Thomas J. Fogarty, M.D. 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.

K884154TRANSLUMINAL ENDARTERECTOMY DEVICEK831809FOGARTY OCCLUDER PADK841310GASTROINTESTINAL DILATORK834451COAXIAL BALLOON GASTROESOPHAGEAL DILAK831384COAXIAL BALLOON URETHRAL DILATOR

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

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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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