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FDA 510(k)

MOBIL-O-GRAPH NG 24 H ABP-CONTROL

K-Number: K072446 · 2007-11-29

ApplicantI.E.M. GmbH
Decision Date2007-11-29
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MOBIL-O-GRAPH NG 24 H ABP-CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is I.E.M. GmbH. It received FDA 510(k) clearance on 2007-11-29 under 510(k) number K072446. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOBIL-O-GRAPH NG 24 H ABP-CONTROL?

MOBIL-O-GRAPH NG 24 H ABP-CONTROL is a medical device that received FDA 510(k) clearance on 2007-11-29. The listed applicant is I.E.M. GmbH. The 510(k) number is K072446.

When did MOBIL-O-GRAPH NG 24 H ABP-CONTROL receive FDA 510(k) clearance?

MOBIL-O-GRAPH NG 24 H ABP-CONTROL received FDA 510(k) clearance on 2007-11-29, under 510(k) number K072446.

Who is the listed applicant for MOBIL-O-GRAPH NG 24 H ABP-CONTROL?

The FDA 510(k) record lists I.E.M. GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOBIL-O-GRAPH NG 24 H ABP-CONTROL?

The FDA product code for MOBIL-O-GRAPH NG 24 H ABP-CONTROL is DXN.

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.

Other records listing I.E.M. GmbH 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.

Related Devices (Code: DXN)

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.

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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