BIFURCATED ALLERGY SKIN TESTING NEEDLE
K-Number: K031630 · 2003-08-07
Advertisement
Device Summary
Frequently Asked Questions
What is the BIFURCATED ALLERGY SKIN TESTING NEEDLE?
BIFURCATED ALLERGY SKIN TESTING NEEDLE is a medical device that received FDA 510(k) clearance on 2003-08-07. The listed applicant is Precision Medical Products, Inc.. The 510(k) number is K031630.
When did BIFURCATED ALLERGY SKIN TESTING NEEDLE receive FDA 510(k) clearance?
BIFURCATED ALLERGY SKIN TESTING NEEDLE received FDA 510(k) clearance on 2003-08-07, under 510(k) number K031630.
Who is the listed applicant for BIFURCATED ALLERGY SKIN TESTING NEEDLE?
The FDA 510(k) record lists Precision Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIFURCATED ALLERGY SKIN TESTING NEEDLE?
The FDA product code for BIFURCATED ALLERGY SKIN TESTING NEEDLE is SCL.
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 Precision Medical 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: SCL)
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