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FDA 510(k)

WRIGHT POCKET DOPPLERS VASCULAR & OBSTETRIC

K-Number: K901015 · 1990-11-05

ApplicantWright Medical Corp.
Decision Date1990-11-05
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WRIGHT POCKET DOPPLERS VASCULAR & OBSTETRIC is the device name listed in this FDA 510(k) record. The listed applicant is Wright Medical Corp.. It received FDA 510(k) clearance on 1990-11-05 under 510(k) number K901015. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WRIGHT POCKET DOPPLERS VASCULAR & OBSTETRIC?

WRIGHT POCKET DOPPLERS VASCULAR & OBSTETRIC is a medical device that received FDA 510(k) clearance on 1990-11-05. The listed applicant is Wright Medical Corp.. The 510(k) number is K901015.

When did WRIGHT POCKET DOPPLERS VASCULAR & OBSTETRIC receive FDA 510(k) clearance?

WRIGHT POCKET DOPPLERS VASCULAR & OBSTETRIC received FDA 510(k) clearance on 1990-11-05, under 510(k) number K901015.

Who is the listed applicant for WRIGHT POCKET DOPPLERS VASCULAR & OBSTETRIC?

The FDA 510(k) record lists Wright Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WRIGHT POCKET DOPPLERS VASCULAR & OBSTETRIC?

The FDA product code for WRIGHT POCKET DOPPLERS VASCULAR & OBSTETRIC is DPW.

Related Clinical Trials

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Other records listing Wright Medical Corp. 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.

K905129BAERVELDT GLAUCOMA IMPLANTK892501WRIGHT MEDICAL FETASAFE

Related Devices (Code: DPW)

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.

K260700BlueDop Vascular ExpertBlueDop Medical, Ltd.K252810FloPatch FP120Flosonics MedicalK251904VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-CP-01, VC-SD-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-SP-01, VC-SD-01)Remington Medical, Inc.K251114FloPatch FP120Flosonics MedicalK243852Elfor-LElfi-Tech , Ltd.K241583VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger (VC-KIT-01, VC-TRX-01, VC-CP-01, VC-CH-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger (VC-KIT-01, VC-TRX-01, VC-SP-01, VC-CH-01)Remington Medical, Inc.

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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