SURGIQUEST ELASTOMERIC OPTICAL TROCAR & CANNULA
K-Number: K063859 · 2007-03-14
Advertisement
Device Summary
Frequently Asked Questions
What is the SURGIQUEST ELASTOMERIC OPTICAL TROCAR & CANNULA?
SURGIQUEST ELASTOMERIC OPTICAL TROCAR & CANNULA is a medical device that received FDA 510(k) clearance on 2007-03-14. The listed applicant is Surgiquest, Inc.. The 510(k) number is K063859.
When did SURGIQUEST ELASTOMERIC OPTICAL TROCAR & CANNULA receive FDA 510(k) clearance?
SURGIQUEST ELASTOMERIC OPTICAL TROCAR & CANNULA received FDA 510(k) clearance on 2007-03-14, under 510(k) number K063859.
Who is the listed applicant for SURGIQUEST ELASTOMERIC OPTICAL TROCAR & CANNULA?
The FDA 510(k) record lists Surgiquest, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SURGIQUEST ELASTOMERIC OPTICAL TROCAR & CANNULA?
The FDA product code for SURGIQUEST ELASTOMERIC OPTICAL TROCAR & CANNULA is GCJ.
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 Surgiquest, 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: GCJ)
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