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FDA 510(k)

MAXI-FLOW SUCTION SET W/Y CONNECTOR

K-Number: K910171 · 1991-02-01

Decision Date1991-02-01
Product CodeGAZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MAXI-FLOW SUCTION SET W/Y CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Adler Instrument Co.. It received FDA 510(k) clearance on 1991-02-01 under 510(k) number K910171. The device is classified under product code GAZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 8 devices →

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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