FLEXIFLO TUBE PLACEMENT VERIFIER
K-Number: K922216 · 1995-01-09
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Device Summary
Frequently Asked Questions
What is the FLEXIFLO TUBE PLACEMENT VERIFIER?
FLEXIFLO TUBE PLACEMENT VERIFIER is a medical device that received FDA 510(k) clearance on 1995-01-09. The listed applicant is Abbott Laboratories. The 510(k) number is K922216.
When did FLEXIFLO TUBE PLACEMENT VERIFIER receive FDA 510(k) clearance?
FLEXIFLO TUBE PLACEMENT VERIFIER received FDA 510(k) clearance on 1995-01-09, under 510(k) number K922216.
Who is the listed applicant for FLEXIFLO TUBE PLACEMENT VERIFIER?
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 TUBE PLACEMENT VERIFIER?
The FDA product code for FLEXIFLO TUBE PLACEMENT VERIFIER 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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