MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002
K-Number: K041852 · 2004-11-15
Advertisement
Device Summary
Frequently Asked Questions
What is the MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002?
MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002 is a medical device that received FDA 510(k) clearance on 2004-11-15. The listed applicant is Minrad, Inc.. The 510(k) number is K041852.
When did MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002 receive FDA 510(k) clearance?
MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002 received FDA 510(k) clearance on 2004-11-15, under 510(k) number K041852.
Who is the listed applicant for MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002?
The FDA 510(k) record lists Minrad, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002?
The FDA product code for MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002 is CCW.
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 Minrad, Inc. 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: CCW)
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