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FDA 510(k)

CANNULA

K-Number: K843187 · 1984-10-31

ApplicantETHICON, Inc.
Decision Date1984-10-31
Product CodeGEA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

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 1984-10-31 under 510(k) number K843187. 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 CANNULA?

CANNULA is a medical device that received FDA 510(k) clearance on 1984-10-31. The listed applicant is ETHICON, Inc.. The 510(k) number is K843187.

When did CANNULA receive FDA 510(k) clearance?

CANNULA received FDA 510(k) clearance on 1984-10-31, under 510(k) number K843187.

Who is the listed applicant for 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 CANNULA?

The FDA product code for CANNULA is GEA.

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Other records listing ETHICON, Inc. 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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