DAVIS+GECK VISADUCT KIT
K-Number: K894685 · 1989-08-22
Advertisement
Device Summary
Frequently Asked Questions
What is the DAVIS+GECK VISADUCT KIT?
DAVIS+GECK VISADUCT KIT is a medical device that received FDA 510(k) clearance on 1989-08-22. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K894685.
When did DAVIS+GECK VISADUCT KIT receive FDA 510(k) clearance?
DAVIS+GECK VISADUCT KIT received FDA 510(k) clearance on 1989-08-22, under 510(k) number K894685.
Who is the listed applicant for DAVIS+GECK VISADUCT KIT?
The FDA 510(k) record lists Davis & Geck, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DAVIS+GECK VISADUCT KIT?
The FDA product code for DAVIS+GECK VISADUCT KIT is LRO.
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 Davis & Geck, 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: LRO)
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