PHILIPS OBTRACEVUE MODEL SW REV. G.00

FDA 510(k) Premarket Notification · Submission K100420 · Applicant: Philips Medizin Systeme Boeblingen GmbH

Public Record 510(k) Submission Decision Date: 2010-07-26 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K100420.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K100420
Device Name
PHILIPS OBTRACEVUE MODEL SW REV. G.00
Product Code
HGM
Decision Date
2010-07-26
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
Obstetrics/Gynecology (OB)
Clearance Type
Abbreviated
Third Party Flag
N
Date Received
2010-02-16

Related Establishments / Registrations

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