RESU-GARD CATHETER SUCTION
K-Number: K902093 · 1990-10-23
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Device Summary
Frequently Asked Questions
What is the RESU-GARD CATHETER SUCTION?
RESU-GARD CATHETER SUCTION is a medical device that received FDA 510(k) clearance on 1990-10-23. The listed applicant is Amg Medical Equipments, Inc.. The 510(k) number is K902093.
When did RESU-GARD CATHETER SUCTION receive FDA 510(k) clearance?
RESU-GARD CATHETER SUCTION received FDA 510(k) clearance on 1990-10-23, under 510(k) number K902093.
Who is the listed applicant for RESU-GARD CATHETER SUCTION?
The FDA 510(k) record lists Amg Medical Equipments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RESU-GARD CATHETER SUCTION?
The FDA product code for RESU-GARD CATHETER SUCTION 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 Amg Medical Equipments, 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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