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FDA 510(k)

AUTO SUTURE ENDOSCOPIC SUCTION/IRRIGATRION DEVICE

K-Number: K903207 · 1990-09-25

ApplicantUnited States Surgical, A Division of Tyco Healthc
Decision Date1990-09-25
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

AUTO SUTURE ENDOSCOPIC SUCTION/IRRIGATRION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is United States Surgical, A Division of Tyco Healthc. It received FDA 510(k) clearance on 1990-09-25 under 510(k) number K903207. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO SUTURE ENDOSCOPIC SUCTION/IRRIGATRION DEVICE?

AUTO SUTURE ENDOSCOPIC SUCTION/IRRIGATRION DEVICE is a medical device that received FDA 510(k) clearance on 1990-09-25. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K903207.

When did AUTO SUTURE ENDOSCOPIC SUCTION/IRRIGATRION DEVICE receive FDA 510(k) clearance?

AUTO SUTURE ENDOSCOPIC SUCTION/IRRIGATRION DEVICE received FDA 510(k) clearance on 1990-09-25, under 510(k) number K903207.

Who is the listed applicant for AUTO SUTURE ENDOSCOPIC SUCTION/IRRIGATRION DEVICE?

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 ENDOSCOPIC SUCTION/IRRIGATRION DEVICE?

The FDA product code for AUTO SUTURE ENDOSCOPIC SUCTION/IRRIGATRION DEVICE is HET.

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Related Devices (Code: HET)

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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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