CONCHA-COLUMN
K-Number: K760866 · 1976-11-01
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Device Summary
Frequently Asked Questions
What is the CONCHA-COLUMN?
CONCHA-COLUMN is a medical device that received FDA 510(k) clearance on 1976-11-01. The listed applicant is Respiratory Care, Inc.. The 510(k) number is K760866.
When did CONCHA-COLUMN receive FDA 510(k) clearance?
CONCHA-COLUMN received FDA 510(k) clearance on 1976-11-01, under 510(k) number K760866.
Who is the listed applicant for CONCHA-COLUMN?
The FDA 510(k) record lists Respiratory Care, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONCHA-COLUMN?
The FDA product code for CONCHA-COLUMN is BTT.
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 Respiratory Care, 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: BTT)
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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