MAXI-FLOW SUCTION SET W/Y CONNECTOR
K-Number: K910171 · 1991-02-01
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Device Summary
Frequently Asked Questions
What is the MAXI-FLOW SUCTION SET W/Y CONNECTOR?
MAXI-FLOW SUCTION SET W/Y CONNECTOR is a medical device that received FDA 510(k) clearance on 1991-02-01. The listed applicant is Adler Instrument Co.. The 510(k) number is K910171.
When did MAXI-FLOW SUCTION SET W/Y CONNECTOR receive FDA 510(k) clearance?
MAXI-FLOW SUCTION SET W/Y CONNECTOR received FDA 510(k) clearance on 1991-02-01, under 510(k) number K910171.
Who is the listed applicant for MAXI-FLOW SUCTION SET W/Y CONNECTOR?
The FDA 510(k) record lists Adler Instrument Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAXI-FLOW SUCTION SET W/Y CONNECTOR?
The FDA product code for MAXI-FLOW SUCTION SET W/Y CONNECTOR is GAZ.
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 Adler Instrument Co. 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: GAZ)
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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