ELIMINATOR BALLOON DILATOR
K-Number: K940965 · 1994-05-20
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Device Summary
Frequently Asked Questions
What is the ELIMINATOR BALLOON DILATOR?
ELIMINATOR BALLOON DILATOR is a medical device that received FDA 510(k) clearance on 1994-05-20. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K940965.
When did ELIMINATOR BALLOON DILATOR receive FDA 510(k) clearance?
ELIMINATOR BALLOON DILATOR received FDA 510(k) clearance on 1994-05-20, under 510(k) number K940965.
Who is the listed applicant for ELIMINATOR BALLOON DILATOR?
The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ELIMINATOR BALLOON DILATOR?
The FDA product code for ELIMINATOR BALLOON DILATOR is FGE.
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 C.R. Bard, 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: FGE)
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.
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