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FDA 510(k)

METANEB

K-Number: K124032 · 2013-04-25

ApplicantHill-Rom Services Pte, Ltd.
Decision Date2013-04-25
Product CodeNHJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

METANEB is the device name listed in this FDA 510(k) record. The listed applicant is Hill-Rom Services Pte, Ltd.. It received FDA 510(k) clearance on 2013-04-25 under 510(k) number K124032. The device is classified under product code NHJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the METANEB?

METANEB is a medical device that received FDA 510(k) clearance on 2013-04-25. The listed applicant is Hill-Rom Services Pte, Ltd.. The 510(k) number is K124032.

When did METANEB receive FDA 510(k) clearance?

METANEB received FDA 510(k) clearance on 2013-04-25, under 510(k) number K124032.

Who is the listed applicant for METANEB?

The FDA 510(k) record lists Hill-Rom Services Pte, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for METANEB?

The FDA product code for METANEB is NHJ.

Related Clinical Trials

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.

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Other records listing Hill-Rom Services Pte, Ltd. 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.

K200988Maximus SystemK192143Maximus SystemK163378Monarch Airway Clearance SystemK151689MetaNeb 4 System

Related Devices (Code: NHJ)

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.

K260604BiWaze Clear SystemAbmrc, LLCK253001KT Airway Clearance Device II (KT-3); KT Airway Clearance Device II (KT-5)Hunan Ruijiong Biotech Co., Ltd.K242438ClearoBreas Medical ABK231728BiWaze Clear SystemAbmrc, LLCK213564BiWaze Clear SystemAbmrc, LLCK200988Maximus SystemHill-Rom Services Pte, Ltd.

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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