MOBIL-O-GRAPH NG 24 H ABP-CONTROL
K-Number: K072446 · 2007-11-29
Advertisement
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement