BEC SHROUDED PLASTIC CANNULA
K-Number: K961328 · 1996-05-30
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Device Summary
Frequently Asked Questions
What is the BEC SHROUDED PLASTIC CANNULA?
BEC SHROUDED PLASTIC CANNULA is a medical device that received FDA 510(k) clearance on 1996-05-30. The listed applicant is Biological & Environmental Control Laboratories. The 510(k) number is K961328.
When did BEC SHROUDED PLASTIC CANNULA receive FDA 510(k) clearance?
BEC SHROUDED PLASTIC CANNULA received FDA 510(k) clearance on 1996-05-30, under 510(k) number K961328.
Who is the listed applicant for BEC SHROUDED PLASTIC CANNULA?
The FDA 510(k) record lists Biological & Environmental Control Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BEC SHROUDED PLASTIC CANNULA?
The FDA product code for BEC SHROUDED PLASTIC CANNULA is FMI.
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 Biological & Environmental Control 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: FMI)
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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