AUTO SUTURE(R) SURGIPORT DISPOS SURG TROCAR/SLEEVE
K-Number: K874879 · 1987-12-17
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Device Summary
Frequently Asked Questions
What is the AUTO SUTURE(R) SURGIPORT DISPOS SURG TROCAR/SLEEVE?
AUTO SUTURE(R) SURGIPORT DISPOS SURG TROCAR/SLEEVE is a medical device that received FDA 510(k) clearance on 1987-12-17. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K874879.
When did AUTO SUTURE(R) SURGIPORT DISPOS SURG TROCAR/SLEEVE receive FDA 510(k) clearance?
AUTO SUTURE(R) SURGIPORT DISPOS SURG TROCAR/SLEEVE received FDA 510(k) clearance on 1987-12-17, under 510(k) number K874879.
Who is the listed applicant for AUTO SUTURE(R) SURGIPORT DISPOS SURG TROCAR/SLEEVE?
The FDA 510(k) record lists United States Surgical, A Division of Tyco Healthc as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AUTO SUTURE(R) SURGIPORT DISPOS SURG TROCAR/SLEEVE?
The FDA product code for AUTO SUTURE(R) SURGIPORT DISPOS SURG TROCAR/SLEEVE is GDH.
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 United States Surgical, A Division of Tyco Healthc 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: GDH)
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.
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