BEC NEEDLELESS INJECTION SITE
K-Number: K961327 · 1996-05-15
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Device Summary
Frequently Asked Questions
What is the BEC NEEDLELESS INJECTION SITE?
BEC NEEDLELESS INJECTION SITE is a medical device that received FDA 510(k) clearance on 1996-05-15. The listed applicant is Biological & Environmental Control Laboratories. The 510(k) number is K961327.
When did BEC NEEDLELESS INJECTION SITE receive FDA 510(k) clearance?
BEC NEEDLELESS INJECTION SITE received FDA 510(k) clearance on 1996-05-15, under 510(k) number K961327.
Who is the listed applicant for BEC NEEDLELESS INJECTION SITE?
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 NEEDLELESS INJECTION SITE?
The FDA product code for BEC NEEDLELESS INJECTION SITE is FPA.
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: FPA)
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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