TRACHEAL SUCTION CATHETER
K-Number: K935600 · 1994-05-10
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Device Summary
Frequently Asked Questions
What is the TRACHEAL SUCTION CATHETER?
TRACHEAL SUCTION CATHETER is a medical device that received FDA 510(k) clearance on 1994-05-10. The listed applicant is Puritas Health Care, Inc.. The 510(k) number is K935600.
When did TRACHEAL SUCTION CATHETER receive FDA 510(k) clearance?
TRACHEAL SUCTION CATHETER received FDA 510(k) clearance on 1994-05-10, under 510(k) number K935600.
Who is the listed applicant for TRACHEAL SUCTION CATHETER?
The FDA 510(k) record lists Puritas Health Care, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRACHEAL SUCTION CATHETER?
The FDA product code for TRACHEAL SUCTION CATHETER is BSY.
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 Puritas Health 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: BSY)
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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