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FDA 510(k)

AUTO SUTURE SURGIPORT CANNULA DIAMETER REDUCER*

K-Number: K896434 · 1989-11-16

ApplicantUnited States Surgical, A Division of Tyco Healthc
Decision Date1989-11-16
Product CodeGEA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AUTO SUTURE SURGIPORT CANNULA DIAMETER REDUCER* 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 1989-11-16 under 510(k) number K896434. The device is classified under product code GEA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO SUTURE SURGIPORT CANNULA DIAMETER REDUCER*?

AUTO SUTURE SURGIPORT CANNULA DIAMETER REDUCER* is a medical device that received FDA 510(k) clearance on 1989-11-16. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K896434.

When did AUTO SUTURE SURGIPORT CANNULA DIAMETER REDUCER* receive FDA 510(k) clearance?

AUTO SUTURE SURGIPORT CANNULA DIAMETER REDUCER* received FDA 510(k) clearance on 1989-11-16, under 510(k) number K896434.

Who is the listed applicant for AUTO SUTURE SURGIPORT CANNULA DIAMETER REDUCER*?

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 SURGIPORT CANNULA DIAMETER REDUCER*?

The FDA product code for AUTO SUTURE SURGIPORT CANNULA DIAMETER REDUCER* is GEA.

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Other records listing United States Surgical, A Division of Tyco Healthc as applicant

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Related Devices (Code: GEA)

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.

K003965MRI SAFE INSTRUMENTSAesculap, Inc.K982472GENICON TROCARGenicon, LCK954599CONMED TROGARD ELECTRONIC TROCAR SYSTEMConmedcorpK922460ORIGIN SECONDARY CANNULA AND TROCAROrigin Medsystems, Inc.K920110ENDOPATH DISPOSABLE THORACIC TROCAR SLEEVEETHICON, Inc.K911262DISPOSABLE SPECIMEN BAG W/CANNULA AND INTRODUCERETHICON, Inc.

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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