FLEXIFLO STOMATE EXTENSION TUBE
K-Number: K902623 · 1991-01-31
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Device Summary
Frequently Asked Questions
What is the FLEXIFLO STOMATE EXTENSION TUBE?
FLEXIFLO STOMATE EXTENSION TUBE is a medical device that received FDA 510(k) clearance on 1991-01-31. The listed applicant is Abbott Laboratories. The 510(k) number is K902623.
When did FLEXIFLO STOMATE EXTENSION TUBE receive FDA 510(k) clearance?
FLEXIFLO STOMATE EXTENSION TUBE received FDA 510(k) clearance on 1991-01-31, under 510(k) number K902623.
Who is the listed applicant for FLEXIFLO STOMATE EXTENSION TUBE?
The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLEXIFLO STOMATE EXTENSION TUBE?
The FDA product code for FLEXIFLO STOMATE EXTENSION TUBE is KNT.
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 Abbott Laboratories 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: KNT)
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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