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FDA 510(k)

FETAL & MATERNAL MONITOR, MODEL F6, F9

K-Number: K082602 · 2008-11-26

ApplicantEdan Instruments, Inc.
Decision Date2008-11-26
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FETAL & MATERNAL MONITOR, MODEL F6, F9 is the device name listed in this FDA 510(k) record. The listed applicant is Edan Instruments, Inc.. It received FDA 510(k) clearance on 2008-11-26 under 510(k) number K082602. The device is classified under product code HGM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FETAL & MATERNAL MONITOR, MODEL F6, F9?

FETAL & MATERNAL MONITOR, MODEL F6, F9 is a medical device that received FDA 510(k) clearance on 2008-11-26. The listed applicant is Edan Instruments, Inc.. The 510(k) number is K082602.

When did FETAL & MATERNAL MONITOR, MODEL F6, F9 receive FDA 510(k) clearance?

FETAL & MATERNAL MONITOR, MODEL F6, F9 received FDA 510(k) clearance on 2008-11-26, under 510(k) number K082602.

Who is the listed applicant for FETAL & MATERNAL MONITOR, MODEL F6, F9?

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

What is the FDA product code for FETAL & MATERNAL MONITOR, MODEL F6, F9?

The FDA product code for FETAL & MATERNAL MONITOR, MODEL F6, F9 is HGM.

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Related Devices (Code: HGM)

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K254036Novii+ Wireless Patch SystemDatex Ohmeda, Inc.K253021ANNE MaternalSibel Health, Inc.K250777Sonicaid Team3Huntleigh Healthcare , Ltd.K241882Fetal & Maternal Monitor (F15A, F15A Air)Edan Instruments, Inc.K241368Sonicaid Team3Huntleigh Healthcare , Ltd.K241009PeriCALM Patterns 3.0Perigen, Inc.

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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