DEFLECTING WIRE GRASPER
K-Number: K903707 · 1990-09-26
Advertisement
Device Summary
Frequently Asked Questions
What is the DEFLECTING WIRE GRASPER?
DEFLECTING WIRE GRASPER is a medical device that received FDA 510(k) clearance on 1990-09-26. The listed applicant is Cook, Inc.. The 510(k) number is K903707.
When did DEFLECTING WIRE GRASPER receive FDA 510(k) clearance?
DEFLECTING WIRE GRASPER received FDA 510(k) clearance on 1990-09-26, under 510(k) number K903707.
Who is the listed applicant for DEFLECTING WIRE GRASPER?
The FDA 510(k) record lists Cook, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEFLECTING WIRE GRASPER?
The FDA product code for DEFLECTING WIRE GRASPER is HCZ.
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 Cook, 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: HCZ)
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