MSI MEDSERV INTERNATIONAL-RIGID ENDOSCOPE
K-Number: K083840 · 2009-09-28
Device Summary
Frequently Asked Questions
What is the MSI MEDSERV INTERNATIONAL-RIGID ENDOSCOPE?
MSI MEDSERV INTERNATIONAL-RIGID ENDOSCOPE is a medical device that received FDA 510(k) clearance on 2009-09-28. The listed applicant is Msi Medserv International Deutschland GmbH. The 510(k) number is K083840.
When did MSI MEDSERV INTERNATIONAL-RIGID ENDOSCOPE receive FDA 510(k) clearance?
MSI MEDSERV INTERNATIONAL-RIGID ENDOSCOPE received FDA 510(k) clearance on 2009-09-28, under 510(k) number K083840.
Who is the listed applicant for MSI MEDSERV INTERNATIONAL-RIGID ENDOSCOPE?
The FDA 510(k) record lists Msi Medserv International Deutschland GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MSI MEDSERV INTERNATIONAL-RIGID ENDOSCOPE?
The FDA product code for MSI MEDSERV INTERNATIONAL-RIGID ENDOSCOPE is GCM.
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.
Related Devices (Code: GCM)
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.