MEDI-VAC FLEXI-CLEAR SUCTION HANDLE
K-Number: K964127 · 1996-12-31
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Device Summary
Frequently Asked Questions
What is the MEDI-VAC FLEXI-CLEAR SUCTION HANDLE?
MEDI-VAC FLEXI-CLEAR SUCTION HANDLE is a medical device that received FDA 510(k) clearance on 1996-12-31. The listed applicant is Allegiance Healthcare Corp.. The 510(k) number is K964127.
When did MEDI-VAC FLEXI-CLEAR SUCTION HANDLE receive FDA 510(k) clearance?
MEDI-VAC FLEXI-CLEAR SUCTION HANDLE received FDA 510(k) clearance on 1996-12-31, under 510(k) number K964127.
Who is the listed applicant for MEDI-VAC FLEXI-CLEAR SUCTION HANDLE?
The FDA 510(k) record lists Allegiance Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDI-VAC FLEXI-CLEAR SUCTION HANDLE?
The FDA product code for MEDI-VAC FLEXI-CLEAR SUCTION HANDLE is GCX.
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 Allegiance Healthcare Corp. 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: GCX)
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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