CONE CATH
K-Number: K931156 · 1993-07-01
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Device Summary
Frequently Asked Questions
What is the CONE CATH?
CONE CATH is a medical device that received FDA 510(k) clearance on 1993-07-01. The listed applicant is Sierra Laboratories, Inc.. The 510(k) number is K931156.
When did CONE CATH receive FDA 510(k) clearance?
CONE CATH received FDA 510(k) clearance on 1993-07-01, under 510(k) number K931156.
Who is the listed applicant for CONE CATH?
The FDA 510(k) record lists Sierra Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONE CATH?
The FDA product code for CONE CATH is EXJ.
Other records listing Sierra Laboratories, 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: EXJ)
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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