STATUS STIK, ACCUSIGN STIK
K-Number: K992068 · 1999-07-06
Advertisement
Device Summary
Frequently Asked Questions
What is the STATUS STIK, ACCUSIGN STIK?
STATUS STIK, ACCUSIGN STIK is a medical device that received FDA 510(k) clearance on 1999-07-06. The listed applicant is Princeton BioMeditech Corp.. The 510(k) number is K992068.
When did STATUS STIK, ACCUSIGN STIK receive FDA 510(k) clearance?
STATUS STIK, ACCUSIGN STIK received FDA 510(k) clearance on 1999-07-06, under 510(k) number K992068.
Who is the listed applicant for STATUS STIK, ACCUSIGN STIK?
The FDA 510(k) record lists Princeton BioMeditech Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STATUS STIK, ACCUSIGN STIK?
The FDA product code for STATUS STIK, ACCUSIGN STIK is DKE.
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 Princeton BioMeditech Corp. 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: DKE)
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