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FDA 510(k)

HANDHELD DOPLER/PEN TRANSDUCER 3MHZ

K-Number: K854590 · 1986-04-23

ApplicantPhilips Medical Systems, Inc.
Decision Date1986-04-23
Product CodeJAF
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HANDHELD DOPLER/PEN TRANSDUCER 3MHZ is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems, Inc.. It received FDA 510(k) clearance on 1986-04-23 under 510(k) number K854590. The device is classified under product code JAF. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HANDHELD DOPLER/PEN TRANSDUCER 3MHZ?

HANDHELD DOPLER/PEN TRANSDUCER 3MHZ is a medical device that received FDA 510(k) clearance on 1986-04-23. The listed applicant is Philips Medical Systems, Inc.. The 510(k) number is K854590.

When did HANDHELD DOPLER/PEN TRANSDUCER 3MHZ receive FDA 510(k) clearance?

HANDHELD DOPLER/PEN TRANSDUCER 3MHZ received FDA 510(k) clearance on 1986-04-23, under 510(k) number K854590.

Who is the listed applicant for HANDHELD DOPLER/PEN TRANSDUCER 3MHZ?

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

What is the FDA product code for HANDHELD DOPLER/PEN TRANSDUCER 3MHZ?

The FDA product code for HANDHELD DOPLER/PEN TRANSDUCER 3MHZ is JAF.

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Other records listing Philips Medical Systems, 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.

K093355PCR ELEVA 1.2K090808PINNACLE3 SMARTARCK071391PHILIPS HEARTSTART 12 LEAD TRANSFER STATION, MODEL 989803142521K063783PHILIPS REUSABLE SPO2 SENSORS M1191T, M1192T AND M1193T, CLIP SENSOR M1196T AND DISPOSABLE SPO2 SENSORS M1131A, M1132AK041741M3290A INTELLIVUE INFORMATION CENTER SOFTWARE RELEASE F.0 AND M4840A PHILIPS TELEMETRY SYSTEM II INCLUDING M4841A PATIENK040955M3290A INTELLIVUE INFORMATION CENTER SOFTWARE RELEASE E.01 AND INTELLIVUE CLINICAL NETWORK ON VLAN

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Related Devices (Code: JAF)

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.

K242487Laminar P1 (LDH-HW-001)Laminar Digital Health, Inc.K110628SIMPLEABINewman MedicalK093393LIFEDOP MODEL 300ABISummit Doppler Systems, Inc.K090009THD SLIDE ONEThd SpaK081429THD SLIDEThd SpaK070815THDG.F. S.R.L.

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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