NEEDLELESS INJECTION SITE
K-Number: K953343 · 1995-10-26
Advertisement
Device Summary
Frequently Asked Questions
What is the NEEDLELESS INJECTION SITE?
NEEDLELESS INJECTION SITE is a medical device that received FDA 510(k) clearance on 1995-10-26. The listed applicant is Medical Associates Network, Inc.. The 510(k) number is K953343.
When did NEEDLELESS INJECTION SITE receive FDA 510(k) clearance?
NEEDLELESS INJECTION SITE received FDA 510(k) clearance on 1995-10-26, under 510(k) number K953343.
Who is the listed applicant for NEEDLELESS INJECTION SITE?
The FDA 510(k) record lists Medical Associates Network, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEEDLELESS INJECTION SITE?
The FDA product code for 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 Medical Associates Network, Inc. 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.
Advertisement