VACUETTE PREMIUM SAFETY NEEDLE SYSTEM
K-Number: K072602 · 2008-06-18
Advertisement
Device Summary
Frequently Asked Questions
What is the VACUETTE PREMIUM SAFETY NEEDLE SYSTEM?
VACUETTE PREMIUM SAFETY NEEDLE SYSTEM is a medical device that received FDA 510(k) clearance on 2008-06-18. The listed applicant is Medpro Safety Products, Inc.. The 510(k) number is K072602.
When did VACUETTE PREMIUM SAFETY NEEDLE SYSTEM receive FDA 510(k) clearance?
VACUETTE PREMIUM SAFETY NEEDLE SYSTEM received FDA 510(k) clearance on 2008-06-18, under 510(k) number K072602.
Who is the listed applicant for VACUETTE PREMIUM SAFETY NEEDLE SYSTEM?
The FDA 510(k) record lists Medpro Safety Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VACUETTE PREMIUM SAFETY NEEDLE SYSTEM?
The FDA product code for VACUETTE PREMIUM SAFETY NEEDLE SYSTEM 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 Medpro Safety Products, 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: 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.
Advertisement