MAXI-FLOW SUCTION SET 12 FT.
K-Number: K910170 · 1991-02-01
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Device Summary
Frequently Asked Questions
What is the MAXI-FLOW SUCTION SET 12 FT.?
MAXI-FLOW SUCTION SET 12 FT. 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 K910170.
When did MAXI-FLOW SUCTION SET 12 FT. receive FDA 510(k) clearance?
MAXI-FLOW SUCTION SET 12 FT. received FDA 510(k) clearance on 1991-02-01, under 510(k) number K910170.
Who is the listed applicant for MAXI-FLOW SUCTION SET 12 FT.?
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 12 FT.?
The FDA product code for MAXI-FLOW SUCTION SET 12 FT. 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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