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)

COX DIAPOSABLE POLYPECTOMY SNARE

K-Number: K912254 · 1991-07-26

Decision Date1991-07-26
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

COX DIAPOSABLE POLYPECTOMY SNARE is the device name listed in this FDA 510(k) record. The listed applicant is Cox Medical Ent., Inc.. It received FDA 510(k) clearance on 1991-07-26 under 510(k) number K912254. The device is classified under product code FDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COX DIAPOSABLE POLYPECTOMY SNARE?

COX DIAPOSABLE POLYPECTOMY SNARE is a medical device that received FDA 510(k) clearance on 1991-07-26. The listed applicant is Cox Medical Ent., Inc.. The 510(k) number is K912254.

When did COX DIAPOSABLE POLYPECTOMY SNARE receive FDA 510(k) clearance?

COX DIAPOSABLE POLYPECTOMY SNARE received FDA 510(k) clearance on 1991-07-26, under 510(k) number K912254.

Who is the listed applicant for COX DIAPOSABLE POLYPECTOMY SNARE?

The FDA 510(k) record lists Cox Medical Ent., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COX DIAPOSABLE POLYPECTOMY SNARE?

The FDA product code for COX DIAPOSABLE POLYPECTOMY SNARE is FDI.

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 Cox Medical Ent., 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 15 devices →

Related Devices (Code: FDI)

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.

↑