FDA 510(k)

UCB

K-Number: K950689 · 1995-03-06

Decision Date1995-03-06

Product CodeMNL

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

UCB 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 1995-03-06 under 510(k) number K950689. The device is classified under product code MNL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UCB?

UCB is a medical device that received FDA 510(k) clearance on 1995-03-06. The listed applicant is Cox Medical Ent., Inc.. The 510(k) number is K950689.

When did UCB receive FDA 510(k) clearance?

UCB received FDA 510(k) clearance on 1995-03-06, under 510(k) number K950689.

Who is the listed applicant for UCB?

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 UCB?

The FDA product code for UCB is MNL.

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.

K946360MODULAR BIOPSY FORCEP K941464BASICS ENDOSCOPY SYSTEM K940911BASICS ENDOSCOPY SYSTEM K932790THERMAL OPTION K935250ACCU-PATH K924655COX DISPOSABLE ENDOSCOPE CLEANING BRUSH(CB-X2)

View all 15 devices →

Related Devices (Code: MNL)

K946293MILL-ROSE SCOPE CLEANING BRUSHMill-Rose Laboratory K892218ENDO-SPONGEEndovations K874239CLEANING BRUSHEndovations

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.