Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DAVIS+GECK VISADUCT KIT

K-Number: K894685 · 1989-08-22

Decision Date1989-08-22
Product CodeLRO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DAVIS+GECK VISADUCT KIT is the device name listed in this FDA 510(k) record. The listed applicant is Davis & Geck, Inc.. It received FDA 510(k) clearance on 1989-08-22 under 510(k) number K894685. The device is classified under product code LRO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 45 devices →

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.

↑