JINOTTI OXYGEN/SUCTION CATHETER
K-Number: K841425 · 1984-09-13
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Device Summary
Frequently Asked Questions
What is the JINOTTI OXYGEN/SUCTION CATHETER?
JINOTTI OXYGEN/SUCTION CATHETER is a medical device that received FDA 510(k) clearance on 1984-09-13. The listed applicant is Research Medical, Inc.. The 510(k) number is K841425.
When did JINOTTI OXYGEN/SUCTION CATHETER receive FDA 510(k) clearance?
JINOTTI OXYGEN/SUCTION CATHETER received FDA 510(k) clearance on 1984-09-13, under 510(k) number K841425.
Who is the listed applicant for JINOTTI OXYGEN/SUCTION CATHETER?
The FDA 510(k) record lists Research Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JINOTTI OXYGEN/SUCTION CATHETER?
The FDA product code for JINOTTI OXYGEN/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 Research Medical, 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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