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FDA 510(k)

PRE-TIED LOOP SUTURE CANNULA

K-Number: K925914 · 1993-05-12

ApplicantETHICON, Inc.
Decision Date1993-05-12
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PRE-TIED LOOP SUTURE CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1993-05-12 under 510(k) number K925914. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRE-TIED LOOP SUTURE CANNULA?

PRE-TIED LOOP SUTURE CANNULA is a medical device that received FDA 510(k) clearance on 1993-05-12. The listed applicant is ETHICON, Inc.. The 510(k) number is K925914.

When did PRE-TIED LOOP SUTURE CANNULA receive FDA 510(k) clearance?

PRE-TIED LOOP SUTURE CANNULA received FDA 510(k) clearance on 1993-05-12, under 510(k) number K925914.

Who is the listed applicant for PRE-TIED LOOP SUTURE CANNULA?

The FDA 510(k) record lists ETHICON, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRE-TIED LOOP SUTURE CANNULA?

The FDA product code for PRE-TIED LOOP SUTURE CANNULA is GCJ.

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Other records listing ETHICON, Inc. as applicant

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Related Devices (Code: GCJ)

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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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